A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1105822



Internal ID15612322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7797538..7887023hg38UCSC Ensembl
Innerchr8:7655060..7744545hg19UCSC Ensembl
Innerchr8:7692470..7781955hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3889486
hg1989486
hg1889486
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610109
Supporting Variants
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, SPAG11A, SPAG11B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1105822
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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