A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556252



Internal ID329393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:147703441..147704070hg38UCSC Ensembl
chr4:148624592..148625221hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16956951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556252
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