A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17644699



Internal ID21836746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31644346..31644496hg38UCSC Ensembl
chr22:32040332..32040482hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6052779
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17644699
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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