A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592669



Internal ID16380078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:184446829..184545885hg38UCSC Ensembl
Innerchr3:184164617..184263673hg19UCSC Ensembl
Innerchr3:185647311..185746367hg18UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3899057
hg1999057
hg1899057
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152557
SamplesNINDS_254
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592669
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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