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Fig. 2 | Molecular Cytogenetics

Fig. 2

From: Identification of a novel deletion mutation in DPY19L2 from an infertile patient with globozoospermia: a case report

Fig. 2

Genome sequencing results of patient samples. a. The results of CNVseq: CNV: copy number variation. b. The domains and mutations inDPY19L2. The DPY19L2 is located on chromosome 12q14.2 and approximately 110.027 kb long. This gene has 22 exons encoding 758 amino acids with a molecular mass of 87.374 kDa. The Chromosome 12q14.2 (g.63950001–64130000) was homozygous deletion of about 180 kb,the mutation leads to complete deletion of DPY19L2

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Molecular Cytogenetics

ISSN: 1755-8166