A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175027



Internal ID15534550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133412162..133563944hg38UCSC Ensembl
Innerchr10:135225666..135377448hg19UCSC Ensembl
Innerchr10:135075656..135227438hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38151783
hg19151783
hg18151783
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552654
Supporting Variants
SamplesNINDS_89
Known GenesCYP2E1, MTG1, SCART1, SPRN, SYCE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175027
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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