A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3684199



Internal ID18635794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18973759..18995594hg38UCSC Ensembl
Innerchr8:18831269..18853104hg19UCSC Ensembl
Innerchr8:18875549..18897384hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3821836
hg1921836
hg1821836
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028621
Supporting Variants
Samples
Known GenesPSD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3684199
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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