A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8648n54



Internal ID22776543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149551336..149552236hg38UCSC Ensembl
chr3:149269123..149270023hg19UCSC Ensembl
chr3:150751813..150752713hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38901
hg19901
hg18901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv592025, nsv592026, nsv592024, nsv592029, nsv592031, nsv592028
Samples
Known GenesWWTR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8648n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss109
Observed Complex0
Frequencyn/a


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