A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590064



Internal ID16377473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:36054449..36226037hg38UCSC Ensembl
Innerchr3:36095941..36267529hg19UCSC Ensembl
Innerchr3:36070945..36242533hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38171589
hg19171589
hg18171589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv962143
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590064
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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