A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525965



Internal ID15106572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:22937442..24358507hg38UCSC Ensembl
Innerchr13:23511581..24932645hg19UCSC Ensembl
Innerchr13:22409581..23830645hg18UCSC Ensembl
Innerchr13:22409581..23830645hg17UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg381421066
hg191421065
hg181421065
hg171421065
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702179
Samples
Known GenesANKRD20A19P, C1QTNF9, C1QTNF9B, C1QTNF9B-AS1, LINC00327, MIPEP, MIR2276, SACS, SACS-AS1, SGCG, SPATA13, SPATA13-AS1, TNFRSF19
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525965
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer