A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1107411



Internal ID15613911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18224320..18409264hg38UCSC Ensembl
Innerchr8:18081829..18266774hg19UCSC Ensembl
Innerchr8:18126109..18311054hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38184945
hg19184946
hg18184946
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610716
Supporting Variants
Samples
Known GenesNAT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1107411
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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