A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18014047



Internal ID20581087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:86803287..88366930hg38UCSC Ensembl
chr13:87455542..89019185hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg381563644
hg191563644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485253
Supporting Variants
Samples
Known GenesLINC00397, MIR4500, MIR4500HG, SLITRK5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18014047
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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