A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522538



Internal ID15103145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94645572..94787706hg38UCSC Ensembl
Innerchr10:96405329..96547463hg19UCSC Ensembl
Innerchr10:96395319..96537453hg18UCSC Ensembl
Innerchr10:96395319..96537453hg17UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38142135
hg19142135
hg18142135
hg17142135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705915
Samples
Known GenesCYP2C18, CYP2C19
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522538
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