A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4956n54



Internal ID22772851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23148644..23149406hg38UCSC Ensembl
chr16:23159965..23160727hg19UCSC Ensembl
chr16:23067466..23068228hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38763
hg19763
hg18763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571681, nsv571682, nsv571678, nsv571684
Samples
Known GenesUSP31
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4956n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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