A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592182



Internal ID16379591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162413620..162520451hg38UCSC Ensembl
Innerchr3:162131408..162238239hg19UCSC Ensembl
Innerchr3:163614102..163720933hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38106832
hg19106832
hg18106832
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8673n54
Supporting Variantsnssv977488
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592182
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer