A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695016



Internal ID15431668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89069113..89123614hg38UCSC Ensembl
Innerchr11:88802281..88856782hg19UCSC Ensembl
Innerchr11:88441929..88496430hg18UCSC Ensembl
Innerchr11:88441929..88496430hg17UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3854502
hg1954502
hg1854502
hg1754502
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522236
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695016
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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