A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591824



Internal ID16032547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:133573902..133574594hg38UCSC Ensembl
Innerchr3:133292746..133293438hg19UCSC Ensembl
Innerchr3:134775436..134776128hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38693
hg19693
hg18693
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8610n54
Supporting Variantsnssv974353, nssv974357, nssv974354, nssv974351, nssv974358, nssv974356, nssv974352, nssv974355, nssv974350
Samples
Known GenesCDV3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591824
Frequency
Sample Size17421
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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