A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277895



Internal ID20844935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38059820..38059973hg38UCSC Ensembl
chr8:37917338..37917491hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556578
Supporting Variants
Samples
Known GenesEIF4EBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277895
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