A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18070444



Internal ID20637484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56687956..56693894hg38UCSC Ensembl
chr20:55263012..55268950hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg385939
hg195939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549510
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18070444
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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