A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261320



Internal ID20470538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27734772..27736234hg38UCSC Ensembl
chr22:28130760..28132222hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg381463
hg191463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747900
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261320
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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