A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589510



Internal ID16376919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6107204..6174524hg38UCSC Ensembl
Innerchr3:6148891..6216211hg19UCSC Ensembl
Innerchr3:6123891..6191211hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3867321
hg1967321
hg1867321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv958261
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589510
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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