A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248726



Internal ID20815766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:174111870..174112315hg38UCSC Ensembl
chr1:174081008..174081453hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38446
hg19446
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544667
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248726
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00041


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