A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528380



Internal ID15455673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:167501580..167506634hg38UCSC Ensembl
Innerchr1:167470817..167475871hg19UCSC Ensembl
Innerchr1:165737441..165742495hg18UCSC Ensembl
Innerchr1:164202475..164207529hg17UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg385055
hg195055
hg185055
hg175055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704969
Samples
Known GenesCD247
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528380
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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