A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041344



Internal ID21950679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34588824..34589098hg38UCSC Ensembl
chr22:34984816..34985090hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648228
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041344
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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