A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589311



Internal ID16030034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:972724..1037340hg38UCSC Ensembl
Innerchr3:1014408..1079024hg19UCSC Ensembl
Innerchr3:989408..1054024hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3864617
hg1964617
hg1864617
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8156n54
Supporting Variantsnssv957819
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589311
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