A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3683731



Internal ID18982012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39372652..39529434hg38UCSC Ensembl
Innerchr8:39230171..39386953hg19UCSC Ensembl
Innerchr8:39349328..39506110hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38156783
hg19156783
hg18156783
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023413
Supporting Variants
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3683731
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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