A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1118226



Internal ID15624726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:103388580..103469507hg38UCSC Ensembl
Innerchr8:104400808..104481735hg19UCSC Ensembl
Innerchr8:104469984..104550911hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3880928
hg1980928
hg1880928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611832
Supporting Variants
Samples
Known GenesDCAF13, SLC25A32
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1118226
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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