A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268573



Internal ID20835613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116143272..116144354hg38UCSC Ensembl
chr6:116464435..116465517hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg381083
hg191083
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561156
Supporting Variants
Samples
Known GenesNT5DC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268573
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00021


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