A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589512



Internal ID16376921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6133543..6208238hg38UCSC Ensembl
Innerchr3:6175230..6249925hg19UCSC Ensembl
Innerchr3:6150230..6224925hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3874696
hg1974696
hg1874696
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8193n54
Supporting Variantsnssv958263
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589512
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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