A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1107394



Internal ID15613894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17787519..17956578hg38UCSC Ensembl
Innerchr8:17645028..17814087hg19UCSC Ensembl
Innerchr8:17689308..17858367hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38169060
hg19169060
hg18169060
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610701
Supporting Variants
Samples
Known GenesFGL1, MTUS1, PCM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1107394
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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