A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693527



Internal ID15430179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:116337679..116370042hg38UCSC Ensembl
Innerchr11:116208396..116240759hg19UCSC Ensembl
Innerchr11:115713606..115745969hg18UCSC Ensembl
Innerchr11:115713606..115745969hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3832364
hg1932364
hg1832364
hg1732364
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516720
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693527
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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