A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203214



Internal ID20770254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21269400..21269681hg38UCSC Ensembl
chr20:21250038..21250319hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526659
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203214
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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