A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18010717



Internal ID20577757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:58864265..58877237hg38UCSC Ensembl
chr13:59438399..59451371hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3812973
hg1912973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495537
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18010717
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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