A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278899



Internal ID20845939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85194073..85198747hg38UCSC Ensembl
chr8:86106308..86110982hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg384675
hg194675
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567367
Supporting Variants
Samples
Known GenesE2F5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278899
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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