A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175067



Internal ID15529476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133492654..133620799hg38UCSC Ensembl
Innerchr10:135306158..135434303hg19UCSC Ensembl
Innerchr10:135156148..135284293hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38128146
hg19128146
hg18128146
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552721
Supporting Variants
SamplesHGDP00791
Known GenesCYP2E1, SPRNP1, SYCE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175067
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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