A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv749990



Internal ID16043946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68827241..68828175hg38UCSC Ensembl
Innerchr10:70586998..70587932hg19UCSC Ensembl
Innerchr10:70257004..70257938hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38935
hg19935
hg18935
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551438
Supporting Variants
Samples
Known GenesSTOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv749990
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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