A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545431



Internal ID20918662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205750270..205751418hg38UCSC Ensembl
chr1:205719398..205720546hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381149
hg191149
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249986
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545431
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