A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17643388



Internal ID21835435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27023651..27023706hg38UCSC Ensembl
chr22:27419614..27419669hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6059274
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17643388
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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