A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592462



Internal ID16379871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:165331163..165565960hg38UCSC Ensembl
Innerchr3:165048951..165283748hg19UCSC Ensembl
Innerchr3:166531645..166766442hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38234798
hg19234798
hg18234798
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153411
Samples1787431197_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592462
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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