A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8644n54



Internal ID22776539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149550714..149551625hg38UCSC Ensembl
chr3:149268501..149269412hg19UCSC Ensembl
chr3:150751191..150752102hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38912
hg19912
hg18912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv592009, nsv592010
Samples
Known GenesWWTR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8644n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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