A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698736



Internal ID15435388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:120918799..120919143hg38UCSC Ensembl
Innerchr11:120789508..120789852hg19UCSC Ensembl
Innerchr11:120294718..120295062hg18UCSC Ensembl
Innerchr11:120294718..120295062hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38345
hg19345
hg18345
hg17345
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523053
Supporting Variants
Samples
Known GenesGRIK4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698736
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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