A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691435



Internal ID15428087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:128212500..128219040hg38UCSC Ensembl
Innerchr11:128082395..128088935hg19UCSC Ensembl
Innerchr11:127587605..127594145hg18UCSC Ensembl
Innerchr11:127587605..127594145hg17UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg386541
hg196541
hg186541
hg176541
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520622
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691435
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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