A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034653



Internal ID18777186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39378072..39537578hg38UCSC Ensembl
Innerchr8:39235591..39395097hg19UCSC Ensembl
Innerchr8:39354748..39514254hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38159507
hg19159507
hg18159507
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7166n100
Supporting Variantsnssv3686425, nssv3686423, nssv3686422, nssv3686424
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)nsv1034653
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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