A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603524



Internal ID21795571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:22818800..22818800hg38UCSC Ensembl
chr16:22830121..22830121hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6090217
Supporting Variants
Samples
Known GenesHS3ST2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603524
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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