A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248252



Internal ID20815292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:200418537..200419612hg38UCSC Ensembl
chr1:200387665..200388740hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381076
hg191076
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552204
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248252
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