A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553073



Internal ID16340482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2156139..2160036hg38UCSC Ensembl
Innerchr11:2177369..2181266hg19UCSC Ensembl
Innerchr11:2133945..2137842hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg383898
hg193898
hg183898
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1566n54
Supporting Variantsnssv764486
Samples
Known GenesINS, INS-IGF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553073
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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