A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520988



Internal ID15101595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:122867102..122918747hg38UCSC Ensembl
Innerchr11:122737810..122789455hg19UCSC Ensembl
Innerchr11:122243020..122294665hg18UCSC Ensembl
Innerchr11:122243020..122294665hg17UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3851646
hg1951646
hg1851646
hg1751646
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694502, nssv680165, nssv679214
Samples
Known GenesC11orf63, CRTAM
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520988
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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