A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8646n54



Internal ID22776541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149550714..149553300hg38UCSC Ensembl
chr3:149268501..149271087hg19UCSC Ensembl
chr3:150751191..150753777hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg382587
hg192587
hg182587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv592027, nsv592023, nsv592030, nsv592016
Samples
Known GenesWWTR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8646n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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