A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551956



Internal ID15992679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94686875..94872496hg38UCSC Ensembl
Innerchr10:96446632..96632253hg19UCSC Ensembl
Innerchr10:96436622..96622243hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38185622
hg19185622
hg18185622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1355n54
Supporting Variantsnssv755897
Samples
Known GenesCYP2C18, CYP2C19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551956
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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