A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1107406



Internal ID15960592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17893228..17895765hg38UCSC Ensembl
Innerchr8:17750737..17753274hg19UCSC Ensembl
Innerchr8:17795017..17797554hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg382538
hg192538
hg182538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610711
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)nssv1107406
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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