A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558189



Internal ID20931260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142217754..142483322hg38UCSC Ensembl
chr8:143299115..143564683hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38265569
hg19265569
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277288
Samples
Known GenesBAI1, TSNARE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558189
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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