A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156382



Internal ID22086783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:119362914..119366180hg38UCSC Ensembl
Outerchr5:119355303..119367387hg38UCSC Ensembl
Innerchr5:118698609..118701875hg19UCSC Ensembl
Outerchr5:118690998..118703082hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3812085
hg1912085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4020207
Samples
Known GenesTNFAIP8
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156382
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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