A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524720



Internal ID15105327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:22120559..22149780hg38UCSC Ensembl
Innerchr8:21978072..22007293hg19UCSC Ensembl
Innerchr8:22034017..22063238hg18UCSC Ensembl
Innerchr8:22034017..22063238hg17UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3829222
hg1929222
hg1829222
hg1729222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700705
Samples
Known GenesHR, LGI3, REEP4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524720
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