A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8701n54



Internal ID20142125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:163001200..163004174hg38UCSC Ensembl
chr3:162718988..162721962hg19UCSC Ensembl
chr3:164201682..164204656hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg382975
hg192975
hg182975
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv592370, nsv592371, nsv592372, nsv592382, nsv592364, nsv592360, nsv592363, nsv592374, nsv592362, nsv592373
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8701n54
Frequency
Sample Size17421
Observed Gain124
Observed Loss387
Observed Complex0
Frequencyn/a


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