A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679214



Internal ID15069180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:122867102..122914109hg38UCSC Ensembl
Innerchr11:122737810..122784817hg19UCSC Ensembl
Innerchr11:122243020..122290027hg18UCSC Ensembl
Innerchr11:122243020..122290027hg17UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3847008
hg1947008
hg1847008
hg1747008
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520988
Supporting Variants
Samples
Known GenesC11orf63, CRTAM
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679214
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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