A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267812



Internal ID20834852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109319612..109320525hg38UCSC Ensembl
chr6:109640815..109641728hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38914
hg19914
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571444
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267812
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