A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526564



Internal ID15107171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:32460401..32462022hg38UCSC Ensembl
Innerchr8:32317917..32319538hg19UCSC Ensembl
Innerchr8:32437459..32439080hg18UCSC Ensembl
Innerchr8:32437459..32439080hg17UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381622
hg191622
hg181622
hg171622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702880
Samples
Known GenesNRG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526564
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