A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068386



Internal ID20635426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46477061..46479793hg38UCSC Ensembl
chr20:45105700..45108432hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg382733
hg192733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544164
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068386
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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