A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250016



Internal ID20817056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207213583..207213902hg38UCSC Ensembl
chr1:207386928..207387247hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547485
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250016
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00142


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