A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247239



Internal ID20814279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106538333..106538906hg38UCSC Ensembl
chr1:107080955..107081528hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539373
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247239
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00043


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer