A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460513



Internal ID238494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43522297..43522393hg38UCSC Ensembl
chr5:43522399..43522495hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16965335
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460513
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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