A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555303



Internal ID16342712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:69076522..69077225hg38UCSC Ensembl
Innerchr11:68843990..68844693hg19UCSC Ensembl
Innerchr11:68600566..68601269hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38704
hg19704
hg18704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1987n54
Supporting Variantsnssv778658, nssv778657
Samples
Known GenesTPCN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555303
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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