A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589298



Internal ID16030021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:643060..1040314hg38UCSC Ensembl
Innerchr3:684744..1081998hg19UCSC Ensembl
Innerchr3:659744..1056998hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38397255
hg19397255
hg18397255
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957809
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589298
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