A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17536373



Internal ID21860728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159000467..159000467hg38UCSC Ensembl
chr1:158970257..158970257hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6051725
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17536373
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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