A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18274845



Internal ID20841885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:86945863..86946911hg38UCSC Ensembl
chr6:87655581..87656629hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg381049
hg191049
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564575
Supporting Variants
Samples
Known GenesHTR1E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18274845
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