A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541592



Internal ID20914874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63946557..63954324hg38UCSC Ensembl
chr20:62577910..62585677hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg387768
hg197768
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203444
Samples
Known GenesUCKL1, UCKL1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541592
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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