A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17540379



Internal ID21864734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:120034357..120037640hg38UCSC Ensembl
chr5:119370052..119373335hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg383284
hg193284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020099
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17540379
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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