A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551960



Internal ID15992683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94740349..94787706hg38UCSC Ensembl
Innerchr10:96500106..96547463hg19UCSC Ensembl
Innerchr10:96490096..96537453hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3847358
hg1947358
hg1847358
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1356n54
Supporting Variantsnssv755901
Samples
Known GenesCYP2C19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551960
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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