A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5999022



Internal ID21908365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17316015..17321454hg38UCSC Ensembl
chr5:17316124..17321563hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg385440
hg195440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540466
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5999022
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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