A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279062



Internal ID20846102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93757452..93757803hg38UCSC Ensembl
chr8:94769680..94770031hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567681
Supporting Variants
Samples
Known GenesTMEM67
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279062
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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