A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277726



Internal ID20844766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30930921..30931735hg38UCSC Ensembl
chr8:30788437..30789251hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38815
hg19815
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568022
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277726
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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