A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17518764



Internal ID21843123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152119791..152120152hg38UCSC Ensembl
chr1:152092267..152092628hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38362
hg19362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981513
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17518764
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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