A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552686



Internal ID15993409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133442823..133543735hg38UCSC Ensembl
Innerchr10:135256327..135357239hg19UCSC Ensembl
Innerchr10:135106317..135207229hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38100913
hg19100913
hg18100913
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1493n54
Supporting Variantsnssv762919
Samples
Known GenesCYP2E1, SCART1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552686
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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