A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520464



Internal ID15101071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:117536418..117577481hg38UCSC Ensembl
Innerchr10:119295929..119336992hg19UCSC Ensembl
Innerchr10:119285919..119326982hg18UCSC Ensembl
Innerchr10:119285919..119326982hg17UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3841064
hg1941064
hg1841064
hg1741064
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697436
Samples
Known GenesEMX2, EMX2OS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520464
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