A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17539503



Internal ID21863858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107405848..107406009hg38UCSC Ensembl
chr5:106741549..106741710hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6015355
Supporting Variants
Samples
Known GenesEFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17539503
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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