A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685493



Internal ID18983774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25133577..25154738hg38UCSC Ensembl
Innerchr8:24991092..25012253hg19UCSC Ensembl
Innerchr8:25047009..25068170hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3821162
hg1921162
hg1821162
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026924
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)nssv3685493
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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