A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558821



Internal ID331874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153436419..153437023hg38UCSC Ensembl
chr5:152815979..152816583hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16976333
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558821
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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