A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018480



Internal ID18761013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7414647..7545918hg38UCSC Ensembl
Innerchr8:7272169..7403440hg19UCSC Ensembl
Innerchr8:7259579..7390850hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38131272
hg19131272
hg18131272
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6939n100
Supporting Variantsnssv3680052
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB4B, 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)nsv1018480
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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