A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558122



Internal ID331196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154667032..154667032hg38UCSC Ensembl
chr5:154046592..154046592hg19UCSC Ensembl
Cytoband5q33.2
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 Variantsnssv16975259
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558122
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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