A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049080



Internal ID21958313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41665749..41666390hg38UCSC Ensembl
chr22:42061753..42062394hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38642
hg19642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649579
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049080
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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