A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459904



Internal ID237909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87038771..87057709hg38UCSC Ensembl
chr5:86334588..86353526hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3818939
hg1918939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16968741
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459904
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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