A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3680621



Internal ID18632216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7533955..7888834hg38UCSC Ensembl
Innerchr8:7391477..7746356hg19UCSC Ensembl
Innerchr8:7378887..7783766hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38354880
hg19354880
hg18404880
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015871
Supporting Variants
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, FAM90A10P, FAM90A7P, PRR23D1, PRR23D2, SPAG11A, SPAG11B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3680621
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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