A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17643821



Internal ID21835868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50742554..50742608hg38UCSC Ensembl
chr22:51180982..51181036hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6046784
Supporting Variants
Samples
Known GenesACR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17643821
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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