A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272980



Internal ID20482198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39101597..39101661hg38UCSC Ensembl
chr22:39497602..39497666hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730281
Supporting Variants
Samples
Known GenesAPOBEC3H
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272980
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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