A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17534390



Internal ID21858746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:184095158..184095825hg38UCSC Ensembl
chr1:184064292..184064959hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38668
hg19668
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982215
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17534390
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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