A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1105778



Internal ID15612278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7482821..7497822hg38UCSC Ensembl
Innerchr8:7340343..7355344hg19UCSC Ensembl
Innerchr8:7327753..7342754hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3815002
hg1915002
hg1815002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610078
Supporting Variants
Samples
Known GenesDEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1105778
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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