A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592716



Internal ID16380125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:187869214..187898074hg38UCSC Ensembl
Innerchr3:187587002..187615862hg19UCSC Ensembl
Innerchr3:189069696..189098556hg18UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3828861
hg1928861
hg1828861
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152569
SamplesHGDP00973
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592716
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