A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17548817



Internal ID21873172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69455616..69464825hg38UCSC Ensembl
chr5:68751443..68760652hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg389210
hg199210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012314
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17548817
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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