A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522189



Internal ID20895550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24904908..24947264hg38UCSC Ensembl
chr20:24885544..24927900hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3842357
hg1942357
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202550
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522189
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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