A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147084



Internal ID346277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:221970613..221974113hg38UCSC Ensembl
chr1:222143955..222147455hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg383501
hg193501
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16897283
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147084
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer