A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066674



Internal ID20633714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18090563..18117745hg38UCSC Ensembl
chr20:18071207..18098389hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3827183
hg1927183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517127
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066674
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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