A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049017



Internal ID21958250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31679682..31679742hg38UCSC Ensembl
chr22:32075668..32075728hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647074
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049017
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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