A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685448



Internal ID18983729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25116916..25149172hg38UCSC Ensembl
Innerchr8:24974431..25006687hg19UCSC Ensembl
Innerchr8:25030348..25062604hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3832257
hg1932257
hg1832257
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023257
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)nssv3685448
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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