A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535867



Internal ID20909221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17460058..17468532hg38UCSC Ensembl
chr22:17939095..17947574hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg388475
hg198480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071588
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535867
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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