A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1107398



Internal ID15613898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17868907..17895765hg38UCSC Ensembl
Innerchr8:17726416..17753274hg19UCSC Ensembl
Innerchr8:17770696..17797554hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3826859
hg1926859
hg1826859
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610705
Supporting Variants
Samples
Known GenesFGL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1107398
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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