A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8282n54



Internal ID22776177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37933442..37945349hg38UCSC Ensembl
chr3:37974933..37986840hg19UCSC Ensembl
chr3:37949937..37961844hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3811908
hg1911908
hg1811908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590073, nsv590075, nsv590074, nsv590068, nsv590069
Samples
Known GenesCTDSPL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8282n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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