A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276066



Internal ID20843106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121321661..121392361hg38UCSC Ensembl
chr8:122333901..122404601hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3870701
hg1970701
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571163
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276066
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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