A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592374



Internal ID16033097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163001313..163004174hg38UCSC Ensembl
Innerchr3:162719101..162721962hg19UCSC Ensembl
Innerchr3:164201795..164204656hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg382862
hg192862
hg182862
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8701n54
Supporting Variantsnssv979827, nssv979830, nssv979831, nssv979834, nssv979829, nssv979832, nssv979835, nssv979828, nssv979833
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592374
Frequency
Sample Size17421
Observed Gain6
Observed Loss3
Observed Complex0
Frequencyn/a


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