A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1987n54



Internal ID22769882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69076522..69077279hg38UCSC Ensembl
chr11:68843990..68844747hg19UCSC Ensembl
chr11:68600566..68601323hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38758
hg19758
hg18758
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555304, nsv555303
Samples
Known GenesTPCN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1987n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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