A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8609n54



Internal ID20142033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133573258..133574774hg38UCSC Ensembl
chr3:133292102..133293618hg19UCSC Ensembl
chr3:134774792..134776308hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381517
hg191517
hg181517
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv591822, nsv591823
Samples
Known GenesCDV3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8609n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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