A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5262n54



Internal ID18997438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84381903..84583279hg38UCSC Ensembl
chr16:84415509..84616885hg19UCSC Ensembl
chr16:82973010..83174386hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38201377
hg19201377
hg18201377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573435, nsv573429
Samples
Known GenesATP2C2, COTL1, TLDC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5262n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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