A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3684178



Internal ID18982459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17756097..17855914hg38UCSC Ensembl
Innerchr8:17613606..17713423hg19UCSC Ensembl
Innerchr8:17657886..17757703hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3899818
hg1999818
hg1899818
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018735
Supporting Variants
Samples
Known GenesMTUS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3684178
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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