A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516555



Internal ID15097162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94774827..94787706hg38UCSC Ensembl
Innerchr10:96534584..96547463hg19UCSC Ensembl
Innerchr10:96524574..96537453hg18UCSC Ensembl
Innerchr10:96524574..96537453hg17UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3812880
hg1912880
hg1812880
hg1712880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv685574, nssv669131
Samples
Known GenesCYP2C19
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516555
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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