A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523622



Internal ID15450915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:28325838..28365626hg38UCSC Ensembl
Innerchr12:28478771..28518559hg19UCSC Ensembl
Innerchr12:28370038..28409826hg18UCSC Ensembl
Innerchr12:28370038..28409826hg17UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3839789
hg1939789
hg1839789
hg1739789
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699419
Samples
Known GenesCCDC91
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523622
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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