A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv749991



Internal ID16043947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68827241..68828278hg38UCSC Ensembl
Innerchr10:70586998..70588035hg19UCSC Ensembl
Innerchr10:70257004..70258041hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381038
hg191038
hg181038
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551439
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)nssv749991
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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