A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5999257



Internal ID21908600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17952321..17952407hg38UCSC Ensembl
chr5:17952430..17952516hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548789
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5999257
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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