A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610101



Internal ID16050824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7788513..7887023hg38UCSC Ensembl
Innerchr8:7646035..7744545hg19UCSC Ensembl
Innerchr8:7683445..7781955hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3898511
hg1998511
hg1898511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11929n54
Supporting Variantsnssv1105810
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)nsv610101
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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