A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524746



Internal ID15452039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63610320..63769686hg38UCSC Ensembl
Innerchr13:64184453..64343819hg19UCSC Ensembl
Innerchr13:63082454..63241820hg18UCSC Ensembl
Innerchr13:63082454..63241820hg17UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38159367
hg19159367
hg18159367
hg17159367
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700737
Samples
Known GenesLINC00395, OR7E156P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524746
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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