A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051668



Internal ID21960901
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 StatusM
Merged Variants
Supporting Variantsnssv17637793
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051668
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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