A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460224



Internal ID238215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112103651..112134564hg38UCSC Ensembl
chr5:111439348..111470261hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3830914
hg1930914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16971925
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460224
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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