A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175068



Internal ID15527487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133538509..133620799hg38UCSC Ensembl
Innerchr10:135352013..135434303hg19UCSC Ensembl
Innerchr10:135202003..135284293hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3882291
hg1982291
hg1882291
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552728
Supporting Variants
SamplesHGDP00475
Known GenesCYP2E1, SPRNP1, SYCE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175068
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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