A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17519123



Internal ID21843482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86976704..86976704hg38UCSC Ensembl
chr1:87442387..87442387hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6058721
Supporting Variants
Samples
Known GenesHS2ST1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17519123
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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