A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544962



Internal ID21869317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:116666885..116693844hg38UCSC Ensembl
chr5:116002581..116029540hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3826960
hg1926960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6018763
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544962
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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