A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271198



Internal ID20838238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33153730..33154810hg38UCSC Ensembl
chr6:33121507..33122587hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg381081
hg191081
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563531
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271198
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