A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589866



Internal ID16377275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:20596736..20676632hg38UCSC Ensembl
Innerchr3:20638228..20718124hg19UCSC Ensembl
Innerchr3:20613232..20693128hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3879897
hg1979897
hg1879897
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151748
SamplesHGDP00645
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589866
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