A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051044



Internal ID21960278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35170722..35171371hg38UCSC Ensembl
chr22:35566715..35567364hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645464
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051044
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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