A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8496n54



Internal ID22776391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105719476..105785285hg38UCSC Ensembl
chr3:105438320..105504129hg19UCSC Ensembl
chr3:106921010..106986819hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3865810
hg1965810
hg1865810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv591244, nsv591246
Samples1780862177_A
Known GenesCBLB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8496n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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