A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4955n54



Internal ID22772850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23148506..23149484hg38UCSC Ensembl
chr16:23159827..23160805hg19UCSC Ensembl
chr16:23067328..23068306hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38979
hg19979
hg18979
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv571679, nsv571685, nsv571676, nsv571683
Samples
Known GenesUSP31
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4955n54
Frequency
Sample Size17421
Observed Gain9
Observed Loss10
Observed Complex0
Frequencyn/a


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