A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027888



Internal ID18770419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39378072..39531498hg38UCSC Ensembl
Innerchr8:39235591..39389017hg19UCSC Ensembl
Innerchr8:39354748..39508174hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38153427
hg19153427
hg18153427
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7166n100
Supporting Variantsnssv3756631, nssv3686219, nssv3686216, nssv3686217, nssv3756630, nssv3686218
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)nsv1027888
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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