A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589627



Internal ID16377036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8784055..8816277hg38UCSC Ensembl
Innerchr3:8825741..8857963hg19UCSC Ensembl
Innerchr3:8800741..8832963hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3832223
hg1932223
hg1832223
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8214n54
Supporting Variantsnssv1151848, nssv1151849, nssv1151847, nssv1151846
SamplesHGDP00143, HGDP00882, HGDP00148, HGDP00341
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589627
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