A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553773



Internal ID16341182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:23980429..24070136hg38UCSC Ensembl
Innerchr11:24001975..24091682hg19UCSC Ensembl
Innerchr11:23958551..24048258hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3889708
hg1989708
hg1889708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1698n54
Supporting Variantsnssv768972
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553773
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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