A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1105858



Internal ID15612358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7851992..7899957hg38UCSC Ensembl
Innerchr8:7709514..7757479hg19UCSC Ensembl
Innerchr8:7746924..7794889hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3847966
hg1947966
hg1847966
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610133
Supporting Variants
Samples
Known GenesDEFB103A, DEFB103B, DEFB4A, SPAG11A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1105858
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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