A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1105808



Internal ID15612308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7773486..8244119hg38UCSC Ensembl
Innerchr8:7631008..8101641hg19UCSC Ensembl
Innerchr8:7668418..8139051hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38470634
hg19470634
hg18470634
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610099
Supporting Variants
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB109P1B, DEFB4A, FAM66E, FAM86B3P, MIR548I3, PRR23D1, PRR23D2, SPAG11A, SPAG11B, USP17L3, USP17L8, ZNF705B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1105808
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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