A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537637



Internal ID20910973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47810649..47814621hg38UCSC Ensembl
chr22:48206398..48210370hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg383973
hg193973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537637
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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