A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696194



Internal ID15432846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6971846..6983663hg38UCSC Ensembl
Innerchr11:6993077..7004894hg19UCSC Ensembl
Innerchr11:6949653..6961470hg18UCSC Ensembl
Innerchr11:6949653..6961470hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3811818
hg1911818
hg1811818
hg1711818
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518745
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696194
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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