A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8149n54



Internal ID22776044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188618..193043hg38UCSC Ensembl
chr3:230301..234726hg19UCSC Ensembl
chr3:205301..209726hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg384426
hg194426
hg184426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589276, nsv589273, nsv589274, nsv589270, nsv589277, nsv589271, nsv589269, nsv589275
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8149n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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