A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567189



Internal ID20940260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:111452461..111458082hg38UCSC Ensembl
chr8:112464690..112470311hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg385622
hg195622
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567189
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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