A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18010344



Internal ID20577384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60931545..60933002hg38UCSC Ensembl
chr13:61505679..61507136hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg381458
hg191458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483500
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18010344
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00268


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