A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610712



Internal ID16398121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17893869..17895765hg38UCSC Ensembl
Innerchr8:17751378..17753274hg19UCSC Ensembl
Innerchr8:17795658..17797554hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381897
hg191897
hg181897
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1107407
Samples
Known GenesFGL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610712
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer