A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526469



Internal ID21850827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:232716729..232717159hg38UCSC Ensembl
chr1:232852475..232852905hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38431
hg19431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5983001
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526469
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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