A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591826



Internal ID16032549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:133573902..133574696hg38UCSC Ensembl
Innerchr3:133292746..133293540hg19UCSC Ensembl
Innerchr3:134775436..134776230hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38795
hg19795
hg18795
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8610n54
Supporting Variantsnssv974365, nssv974366
Samples
Known GenesCDV3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591826
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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