A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589882



Internal ID16377291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21041604..21137840hg38UCSC Ensembl
Innerchr3:21083096..21179332hg19UCSC Ensembl
Innerchr3:21058100..21154336hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3896237
hg1996237
hg1896237
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8255n54
Supporting Variantsnssv959903, nssv959905, nssv959904, nssv1151750
SamplesHGDP00864
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589882
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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