A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8284n54



Internal ID22776179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37940970..37943926hg38UCSC Ensembl
chr3:37982461..37985417hg19UCSC Ensembl
chr3:37957465..37960421hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg382957
hg192957
hg182957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590087, nsv590081, nsv590080, nsv590079
Samples
Known GenesCTDSPL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8284n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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