A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589620



Internal ID16377029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8779046..8812029hg38UCSC Ensembl
Innerchr3:8820732..8853715hg19UCSC Ensembl
Innerchr3:8795732..8828715hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3832984
hg1932984
hg1832984
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8214n54
Supporting Variantsnssv1151839
Samples1780854401_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589620
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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