A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8349n54



Internal ID22776244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63286292..63287392hg38UCSC Ensembl
chr3:63271968..63273068hg19UCSC Ensembl
chr3:63247008..63248108hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg381101
hg191101
hg181101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590450, nsv590451, nsv590449, nsv590452, nsv590453
Samples
Known GenesSYNPR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8349n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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