A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9182n54



Internal ID22777077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102859340..102861607hg38UCSC Ensembl
chr4:103780497..103782764hg19UCSC Ensembl
chr4:103999596..104001853hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg382268
hg192268
hg182258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv594960, nsv594958, nsv594959
Samples
Known GenesUBE2D3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9182n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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