A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059980



Internal ID21969214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38344470..38345570hg38UCSC Ensembl
chr22:38740475..38741575hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645320
Samples
Known GenesLOC400927
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059980
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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