A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv752119



Internal ID16046075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82591121..83412579hg38UCSC Ensembl
Innerchr10:84350877..85172335hg19UCSC Ensembl
Innerchr10:84340857..85162315hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38821459
hg19821459
hg18821459
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551733
Supporting Variants
Samples
Known GenesNRG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv752119
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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