A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8290n54



Internal ID22776185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41318043..41783064hg38UCSC Ensembl
chr3:41359534..41824556hg19UCSC Ensembl
chr3:41334538..41799560hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38465022
hg19465023
hg18465023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590119, nsv590120, nsv590122, nsv590121
Samples1798860049_A
Known GenesULK4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8290n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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