A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558193



Internal ID20931264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115064074..115064507hg38UCSC Ensembl
chr8:116076303..116076736hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7472n223
Supporting Variantsnssv18277002
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558193
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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