A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698709



Internal ID15088675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55755253..55755908hg38UCSC Ensembl
Innerchr11:55522729..55523384hg19UCSC Ensembl
Innerchr11:55279305..55279960hg18UCSC Ensembl
Innerchr11:55279305..55279960hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38656
hg19656
hg18656
hg17656
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517440
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698709
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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