A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8526n54



Internal ID20141950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122181001..122216999hg38UCSC Ensembl
chr3:121899848..121935846hg19UCSC Ensembl
chr3:123382538..123418536hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3835999
hg1935999
hg1835999
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv591408, nsv591403, nsv591405, nsv591404
Samples
Known GenesCASR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8526n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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