A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645614



Internal ID21837661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30454865..30454931hg38UCSC Ensembl
chr22:30850852..30850918hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6058963
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645614
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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