A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523565



Internal ID15450858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145716152..145764299hg38UCSC Ensembl
Innerchr3:145433939..145482086hg19UCSC Ensembl
Innerchr3:146916629..146964776hg18UCSC Ensembl
Innerchr3:146916637..146964784hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3848148
hg1948148
hg1848148
hg1748148
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699346
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523565
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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