A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174566



Internal ID15528328
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 StatusS
Merged Variantsnsv551964
Supporting Variants
SamplesHGDP00622
Known GenesCYP2C8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174566
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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