A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591813



Internal ID16032536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:133414251..133418117hg38UCSC Ensembl
Innerchr3:133133095..133136961hg19UCSC Ensembl
Innerchr3:134615785..134619651hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg383867
hg193867
hg183867
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8608n54
Supporting Variantsnssv974239, nssv974236, nssv974237, nssv974234, nssv974232, nssv974240, nssv974235, nssv974230, nssv974233, nssv974238, nssv974231
Samples
Known GenesBFSP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591813
Frequency
Sample Size17421
Observed Gain3
Observed Loss8
Observed Complex0
Frequencyn/a


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