A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702966



Internal ID15439618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3236606..3244721hg38UCSC Ensembl
Innerchr11:3257836..3265951hg19UCSC Ensembl
Innerchr11:3214412..3222527hg18UCSC Ensembl
Innerchr11:3214412..3222527hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg388116
hg198116
hg188116
hg178116
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526641
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702966
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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