A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9185n54



Internal ID22777080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102860417..102862255hg38UCSC Ensembl
chr4:103781574..103783412hg19UCSC Ensembl
chr4:104000669..104002501hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg381839
hg191839
hg181833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv594976, nsv594974, nsv594972, nsv594971, nsv594977, nsv594969, nsv594975
Samples
Known GenesUBE2D3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9185n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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