A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554795



Internal ID327969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154997783..155063938hg38UCSC Ensembl
chr3:154715572..154781727hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3866156
hg1966156
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16941894
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554795
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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