A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3666896



Internal ID18965177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12407033..12496209hg38UCSC Ensembl
Innerchr8:12264542..12353718hg19UCSC Ensembl
Innerchr8:12308913..12398089hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3889177
hg1989177
hg1889177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029359
Supporting Variants
Samples
Known GenesFAM66A, FAM86B2, FAM90A25P, LOC100506990
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3666896
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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