A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559666



Internal ID20932737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:54011885..54012835hg38UCSC Ensembl
chr5:53307715..53308665hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38951
hg19951
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269065
Samples
Known GenesARL15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559666
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