A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248249



Internal ID20815289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:200347034..200347574hg38UCSC Ensembl
chr1:200316162..200316702hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546282
Supporting Variants
Samples
Known GenesLINC00862
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248249
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