A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264153



Internal ID20831193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:116884639..117230294hg38UCSC Ensembl
chr4:117805795..118151450hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38345656
hg19345656
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573346
Supporting Variants
Samples
Known GenesTRAM1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264153
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