A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524719



Internal ID15452012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:133374456..133399854hg38UCSC Ensembl
Innerchr8:134386699..134412097hg19UCSC Ensembl
Innerchr8:134455881..134481279hg18UCSC Ensembl
Innerchr8:134455881..134481279hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3825399
hg1925399
hg1825399
hg1725399
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700704
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524719
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