A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3687602



Internal ID18639197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39378072..39540952hg38UCSC Ensembl
Innerchr8:39235591..39398471hg19UCSC Ensembl
Innerchr8:39354748..39517628hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38162881
hg19162881
hg18162881
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021805
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)nssv3687602
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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