A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589442



Internal ID16376851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4140066..4271051hg38UCSC Ensembl
Innerchr3:4181750..4312735hg19UCSC Ensembl
Innerchr3:4156750..4287735hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38130986
hg19130986
hg18130986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8183n54
Supporting Variantsnssv958039, nssv958040, nssv1152462, nssv1152463, nssv958038, nssv958041
Samples1780854417_A, 1798860491_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589442
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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