A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586936



Internal ID20960007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13321760..13322433hg38UCSC Ensembl
chr18:13321759..13322432hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38674
hg19674
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243473
Samples
Known GenesLDLRAD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586936
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