A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3682942



Internal ID18634537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39378072..39527663hg38UCSC Ensembl
Innerchr8:39235591..39385182hg19UCSC Ensembl
Innerchr8:39354748..39504339hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38149592
hg19149592
hg18149592
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017106
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)nssv3682942
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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