A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205283



Internal ID20772323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51580360..51589734hg38UCSC Ensembl
chr20:50196899..50206273hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg389375
hg199375
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549604
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205283
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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