A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3684190



Internal ID18982471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18102163..18136829hg38UCSC Ensembl
Innerchr8:17959672..17994338hg19UCSC Ensembl
Innerchr8:18003952..18038618hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3834667
hg1934667
hg1834667
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024294
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3684190
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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