A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672211



Internal ID21620516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149817539..149876316hg38UCSC Ensembl
chr1:149789093..149847866hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3858778
hg1958774
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17060618
Samples
Known GenesHIST2H2AA3, HIST2H2AA4, HIST2H2BC, HIST2H3A, HIST2H3C, HIST2H4A, HIST2H4B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672211
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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