A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460901



Internal ID238868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:26431414..26432670hg38UCSC Ensembl
chr5:26431523..26432779hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg381257
hg191257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16963843
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460901
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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