A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540741



Internal ID20914031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42775960..42810225hg38UCSC Ensembl
chr22:43171966..43206231hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3834266
hg1934266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074353
Samples
Known GenesARFGAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540741
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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