A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551964



Internal ID15992687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:95045614..95102529hg38UCSC Ensembl
Innerchr10:96805371..96862286hg19UCSC Ensembl
Innerchr10:96795361..96852276hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3856916
hg1956916
hg1856916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174566
SamplesHGDP00622
Known GenesCYP2C8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551964
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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