A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534993



Internal ID20908354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36567961..36571149hg38UCSC Ensembl
chr20:35196364..35199552hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg383189
hg193189
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534993
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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