A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027693



Internal ID18770225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39378072..39538326hg38UCSC Ensembl
Innerchr8:39235591..39395845hg19UCSC Ensembl
Innerchr8:39354748..39515002hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38160255
hg19160255
hg18160255
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7166n100
Supporting Variantsnssv3686430, nssv3686428, nssv3686429, nssv3686427, nssv3686431, nssv3686426, nssv3756649
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)nsv1027693
Frequency
Sample Size29084
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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