A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103794



Internal ID22013027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187413745..187424394hg38UCSC Ensembl
chr3:187131533..187142182hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3810650
hg1910650
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557489
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103794
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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