A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572426



Internal ID20945497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108196871..108197411hg38UCSC Ensembl
chr4:109118027..109118567hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263477
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572426
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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