A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277026



Internal ID20844066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116747363..116747765hg38UCSC Ensembl
chr8:117759602..117760004hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569956
Supporting Variants
Samples
Known GenesEIF3H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277026
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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