A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3666879



Internal ID18965160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12403406..12634130hg38UCSC Ensembl
Innerchr8:12260915..12491639hg19UCSC Ensembl
Innerchr8:12305286..12536010hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38230725
hg19230725
hg18230725
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029482
Supporting Variants
Samples
Known GenesFAM66A, FAM86B2, FAM90A25P, LOC100506990, LOC729732
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3666879
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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