A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv744256



Internal ID16038212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:18562406..18569274hg38UCSC Ensembl
Innerchr10:18851335..18858203hg19UCSC Ensembl
Innerchr10:18891341..18898209hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg386869
hg196869
hg186869
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550102
Supporting Variants
Samples
Known GenesNSUN6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv744256
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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