A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196308



Internal ID20763348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85749741..85758581hg38UCSC Ensembl
chr13:86323876..86332716hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg388841
hg198841
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485979
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196308
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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