A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638656



Internal ID21830703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:20329140..20343459hg38UCSC Ensembl
chr22:20316663..20330982hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3814320
hg1914320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6058315
Supporting Variants
Samples
Known GenesLOC729444
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638656
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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