A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147326



Internal ID346508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155158164..155173920hg38UCSC Ensembl
chr5:154537724..154553480hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3815757
hg1915757
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977332
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147326
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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