A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517308



Internal ID15444601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:87967474..87967640hg38UCSC Ensembl
Innerchr11:87678366..87678532hg19UCSC Ensembl
Innerchr11:87356014..87356180hg18UCSC Ensembl
Innerchr11:87356014..87356180hg17UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38167
hg19167
hg18167
hg17167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv651668, nssv685032, nssv693849
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517308
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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