A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540545



Internal ID20913838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34424998..34429844hg38UCSC Ensembl
chr22:34820988..34825835hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg384847
hg194848
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204588
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540545
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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