A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460940



Internal ID238905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160226509..160227397hg38UCSC Ensembl
chr5:159653516..159654404hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38889
hg19889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16976005
Samples
Known GenesFABP6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460940
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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