A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066604



Internal ID20633644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16752682..16753395hg38UCSC Ensembl
chr20:16733327..16734040hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38714
hg19714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524660
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066604
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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