A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521536



Internal ID15448829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:101615074..101671867hg38UCSC Ensembl
Innerchr13:102267424..102324217hg19UCSC Ensembl
Innerchr13:101065425..101122218hg18UCSC Ensembl
Innerchr13:101065425..101122218hg17UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3856794
hg1956794
hg1856794
hg1756794
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698152
Samples
Known GenesITGBL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521536
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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