A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589275



Internal ID16376684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:188773..192407hg38UCSC Ensembl
Innerchr3:230456..234090hg19UCSC Ensembl
Innerchr3:205456..209090hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg383635
hg193635
hg183635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8149n54
Supporting Variantsnssv957779, nssv957781, nssv957780, nssv957778, nssv957782
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589275
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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