A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17553974



Internal ID21878329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:89909019..89909131hg38UCSC Ensembl
chr5:89204836..89204948hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013876
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17553974
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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