A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563998



Internal ID336922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161632470..161632470hg38UCSC Ensembl
chr5:161059476..161059476hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg381
hg191
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977478
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563998
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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