A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589418



Internal ID16376827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4046892..4066953hg38UCSC Ensembl
Innerchr3:4088576..4108637hg19UCSC Ensembl
Innerchr3:4063576..4083637hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3820062
hg1920062
hg1820062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv958019
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589418
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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