A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271910



Internal ID20838950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:133836938..133838628hg38UCSC Ensembl
chr6:134158076..134159766hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg381691
hg191691
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568013
Supporting Variants
Samples
Known GenesMGC34034
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271910
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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