A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553858



Internal ID16341267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25096205..25153652hg38UCSC Ensembl
Innerchr11:25117751..25175198hg19UCSC Ensembl
Innerchr11:25074327..25131774hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3857448
hg1957448
hg1857448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174764
SamplesHGDP00941
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553858
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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