A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553076



Internal ID16340485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2158083..2160831hg38UCSC Ensembl
Innerchr11:2179313..2182061hg19UCSC Ensembl
Innerchr11:2135889..2138637hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382749
hg192749
hg182749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv764489
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)nsv553076
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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