A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526668



Internal ID15453961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:100153543..100160601hg38UCSC Ensembl
Innerchr13:100805797..100812855hg19UCSC Ensembl
Innerchr13:99603798..99610856hg18UCSC Ensembl
Innerchr13:99603798..99610856hg17UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg387059
hg197059
hg187059
hg177059
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702998
Samples
Known GenesPCCA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526668
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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