A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663334



Internal ID15399986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:56902354..56936567hg38UCSC Ensembl
Innerchr11:56669830..56704042hg19UCSC Ensembl
Innerchr11:56426406..56460618hg18UCSC Ensembl
Innerchr11:56426406..56460618hg17UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3834214
hg1934213
hg1834213
hg1734213
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520375
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663334
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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