A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175071



Internal ID15531393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133538596..133591032hg38UCSC Ensembl
Innerchr10:135352100..135404536hg19UCSC Ensembl
Innerchr10:135202090..135254526hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3852437
hg1952437
hg1852437
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552729
Supporting Variants
SamplesHGDP01091
Known GenesCYP2E1, SPRNP1, SYCE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175071
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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