A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559219



Internal ID332260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162553436..162553453hg38UCSC Ensembl
chr5:161980442..161980459hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3818
hg1918
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16976506
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559219
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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