A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591748



Internal ID20964819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:28159785..28161363hg38UCSC Ensembl
chr18:25739749..25741327hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg381579
hg191579
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243981
Samples
Known GenesCDH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591748
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