A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542873



Internal ID20916124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47378499..47386834hg38UCSC Ensembl
chr20:46007243..46015578hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg388336
hg198336
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202924
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542873
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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