A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459352



Internal ID237368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:89707903..89708226hg38UCSC Ensembl
chr5:89003720..89004043hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16968932
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459352
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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