A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275460



Internal ID20484678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22844989..22845486hg38UCSC Ensembl
chr16:22856310..22856807hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746820
Supporting Variants
Samples
Known GenesHS3ST2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275460
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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