A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066639



Internal ID20633679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:17142261..17143006hg38UCSC Ensembl
chr20:17122906..17123651hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38746
hg19746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526956
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066639
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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