A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592249



Internal ID16379658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162794895..163004174hg38UCSC Ensembl
Innerchr3:162512683..162721962hg19UCSC Ensembl
Innerchr3:163995377..164204656hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38209280
hg19209280
hg18209280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8679n54
Supporting Variantsnssv978180, nssv978175, nssv978170, nssv978177, nssv978183, nssv978185, nssv978186, nssv978194, nssv978178, nssv978193, nssv978174, nssv978166, nssv978192, nssv978182, nssv978196, nssv978165, nssv978171, nssv978169, nssv978176, nssv978190, nssv978191, nssv978195, nssv978167, nssv978179, nssv978184, nssv978187, nssv978168, nssv978172, nssv978197, nssv978181, nssv978189, nssv978188, nssv978173
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592249
Frequency
Sample Size17421
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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