A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018189



Internal ID19107406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7397576..7785611hg38UCSC Ensembl
Innerchr8:7255098..7643133hg19UCSC Ensembl
Innerchr8:7242508..7680543hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38388036
hg19388036
hg18438036
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6908n100
Supporting Variantsnssv3679694
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB4B, FAM90A10P, FAM90A7P, PRR23D1, PRR23D2, SPAG11B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018189
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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