A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3674903



Internal ID18626498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:96386..458905hg38UCSC Ensembl
Innerchr8:46386..408905hg19UCSC Ensembl
Innerchr8:36386..398905hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38362520
hg19362520
hg18362520
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029069
Supporting Variants
Samples
Known GenesFAM87A, FBXO25, OR4F21, RPL23AP53, ZNF596
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3674903
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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