A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696975



Internal ID15433627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8332388..8334366hg38UCSC Ensembl
Innerchr11:8353935..8355913hg19UCSC Ensembl
Innerchr11:8310511..8312489hg18UCSC Ensembl
Innerchr11:8310511..8312489hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381979
hg191979
hg181979
hg171979
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519655
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696975
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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