A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17637793



Internal ID21829840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35502373..35502532hg38UCSC Ensembl
chr22:35898420..35898579hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6051668
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17637793
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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