A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461771



Internal ID239717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14528062..14534086hg38UCSC Ensembl
chr5:14528171..14534195hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg386025
hg196025
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16962676
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461771
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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