A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8747n54



Internal ID22776642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:176088947..176183792hg38UCSC Ensembl
chr3:175806735..175901580hg19UCSC Ensembl
chr3:177289429..177384274hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3894846
hg1994846
hg1894846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv592603, nsv592605, nsv592604
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8747n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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