A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610708



Internal ID16398117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17892721..17895638hg38UCSC Ensembl
Innerchr8:17750230..17753147hg19UCSC Ensembl
Innerchr8:17794510..17797427hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg382918
hg192918
hg182918
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12045n54
Supporting Variantsnssv1107401
Samples
Known GenesFGL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610708
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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