A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266129



Internal ID20833169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99377634..99378215hg38UCSC Ensembl
chr4:100298791..100299372hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564504
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266129
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