A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1113884



Internal ID15967070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:43576082..43937428hg38UCSC Ensembl
Innerchr8:43431225..43792571hg19UCSC Ensembl
Innerchr8:43550382..43911728hg18UCSC Ensembl
Cytoband8p11.1
Allele length
AssemblyAllele length
hg38361347
hg19361347
hg18361347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611153
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1113884
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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