A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520174



Internal ID15447467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145507323..145536355hg38UCSC Ensembl
Innerchr3:145225110..145254142hg19UCSC Ensembl
Innerchr3:146707800..146736832hg18UCSC Ensembl
Innerchr3:146707808..146736840hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3829033
hg1929033
hg1829033
hg1729033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673241, nssv682932, nssv685144, nssv687481, nssv681141, nssv661350
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520174
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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