A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625962



Internal ID21818009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26090287..26101956hg38UCSC Ensembl
chr16:26101608..26113277hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3811670
hg1911670
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6110698
Supporting Variants
Samples
Known GenesHS3ST4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625962
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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