A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1105839



Internal ID15612339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7829864..7935485hg38UCSC Ensembl
Innerchr8:7687386..7793007hg19UCSC Ensembl
Innerchr8:7724796..7830417hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38105622
hg19105622
hg18105622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610121
Supporting Variants
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB4A, SPAG11A, SPAG11B, ZNF705B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1105839
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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