A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589726



Internal ID16377135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:13094000..13125418hg38UCSC Ensembl
Innerchr3:13135500..13166918hg19UCSC Ensembl
Innerchr3:13110500..13141918hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3831419
hg1931419
hg1831419
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959137
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589726
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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