A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266576



Internal ID20833616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:83041510..83044419hg38UCSC Ensembl
chr4:83962663..83965572hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg382910
hg192910
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572949
Supporting Variants
Samples
Known GenesCOPS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266576
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