A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273366



Internal ID20840406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26380551..26381005hg38UCSC Ensembl
chr7:26420171..26420625hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564324
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273366
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