A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455642



Internal ID233719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155762841..155762949hg38UCSC Ensembl
chr5:155189851..155189959hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16975870
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455642
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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