A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584582



Internal ID20957653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50945283..50945817hg38UCSC Ensembl
chr18:48471653..48472187hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38535
hg19535
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244620
Samples
Known GenesME2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584582
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