A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8287n54



Internal ID20141711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39146691..39189506hg38UCSC Ensembl
chr3:39188182..39230997hg19UCSC Ensembl
chr3:39163186..39206001hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3842816
hg1942816
hg1842816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590105, nsv590103, nsv590104
Samples
Known GenesCSRNP1, XIRP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8287n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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