A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571016



Internal ID20944087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100303709..100304062hg38UCSC Ensembl
chr8:101315937..101316290hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275887
Samples
Known GenesRNF19A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571016
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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