A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244749



Internal ID20811789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70252416..70256121hg38UCSC Ensembl
chr18:67919652..67923357hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg383706
hg193706
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596016
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244749
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