A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202931



Internal ID20769971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4748650..4758087hg38UCSC Ensembl
chr20:4729296..4738733hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg389438
hg199438
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534499
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202931
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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