A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610710



Internal ID16398119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17892819..17895765hg38UCSC Ensembl
Innerchr8:17750328..17753274hg19UCSC Ensembl
Innerchr8:17794608..17797554hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg382947
hg192947
hg182947
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12045n54
Supporting Variantsnssv1107405, nssv1107404, nssv1107403
Samples
Known GenesFGL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610710
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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