A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526172



Internal ID15453465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70687977..70744387hg38UCSC Ensembl
Innerchr15:70980316..71036726hg19UCSC Ensembl
Innerchr15:68767370..68823780hg18UCSC Ensembl
Innerchr15:68767370..68823780hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3856411
hg1956411
hg1856411
hg1756411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702433
Samples
Known GenesUACA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526172
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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