A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068570



Internal ID20635610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62932244..62933941hg38UCSC Ensembl
chr20:61563596..61565293hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381698
hg191698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543382
Supporting Variants
Samples
Known GenesDIDO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068570
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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