A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242581



Internal ID20809621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62430845..62433326hg38UCSC Ensembl
chr17:60508206..60510687hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg382482
hg192482
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579355
Supporting Variants
Samples
Known GenesMETTL2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242581
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer