A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17524592



Internal ID21848950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:232262683..232262683hg38UCSC Ensembl
chr1:232398429..232398429hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6043520
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17524592
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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