A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8664n54



Internal ID22776559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:162136930..162238888hg38UCSC Ensembl
chr3:161854718..161956676hg19UCSC Ensembl
chr3:163337412..163439370hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38101959
hg19101959
hg18101959
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv592148, nsv592149, nsv592150, nsv592152, nsv592147
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8664n54
Frequency
Sample Size17421
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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