A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592450



Internal ID16033173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164988854..165078852hg38UCSC Ensembl
Innerchr3:164706642..164796640hg19UCSC Ensembl
Innerchr3:166189336..166279334hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3889999
hg1989999
hg1889999
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv981124
Samples
Known GenesSI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592450
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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