A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526320



Internal ID15453613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:58225805..58235697hg38UCSC Ensembl
Innerchr8:59138364..59148256hg19UCSC Ensembl
Innerchr8:59300918..59310810hg18UCSC Ensembl
Innerchr8:59300918..59310810hg17UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg389893
hg199893
hg189893
hg179893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702608
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526320
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