A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553952



Internal ID16341361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31370402..31374992hg38UCSC Ensembl
Innerchr11:31391949..31396539hg19UCSC Ensembl
Innerchr11:31348525..31353115hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg384591
hg194591
hg184591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1734n54
Supporting Variantsnssv770677, nssv770678, nssv770676
Samples
Known GenesDNAJC24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553952
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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