A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273850



Internal ID20840890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17926670..17927264hg38UCSC Ensembl
chr7:17966293..17966887hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563180
Supporting Variants
Samples
Known GenesSNX13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273850
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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