A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191867



Internal ID20758907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:81866101..81872400hg38UCSC Ensembl
chr13:82440236..82446535hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg386300
hg196300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480498
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191867
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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