A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553074



Internal ID16340483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2157278..2159919hg38UCSC Ensembl
Innerchr11:2178508..2181149hg19UCSC Ensembl
Innerchr11:2135084..2137725hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg382642
hg192642
hg182642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1567n54
Supporting Variantsnssv764487
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)nsv553074
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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