A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698234



Internal ID15434886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11102109..11145046hg38UCSC Ensembl
Innerchr11:11123656..11166593hg19UCSC Ensembl
Innerchr11:11080232..11123169hg18UCSC Ensembl
Innerchr11:11080232..11123169hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3842938
hg1942938
hg1842938
hg1742938
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521616
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698234
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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