A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515707



Internal ID15443318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:128097459..128116307hg38UCSC Ensembl
Innerchr11:127967354..127986202hg19UCSC Ensembl
Innerchr11:127472564..127491412hg18UCSC Ensembl
Innerchr11:127472564..127491412hg17UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3818849
hg1918849
hg1818849
hg1718849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv683736, nssv665407, nssv661625, nssv681074, nssv658184, nssv660617, nssv653355, nssv679638, nssv651886, nssv681637, nssv662806, nssv666775, nssv690847, nssv668167, nssv659958, nssv693275
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515707
Frequency
Sample Size2026
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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