A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764483



Internal ID16058439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2154812..2177188hg38UCSC Ensembl
Innerchr11:2176042..2198418hg19UCSC Ensembl
Innerchr11:2132618..2154994hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3822377
hg1922377
hg1822377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553070
Supporting Variants
Samples
Known GenesINS, INS-IGF2, MIR4686, TH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv764483
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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