A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271441



Internal ID20838481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41231050..41232586hg38UCSC Ensembl
chr6:41198788..41200324hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381537
hg191537
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559522
Supporting Variants
Samples
Known GenesTREML4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271441
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