A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564640



Internal ID20937711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26368888..26369626hg38UCSC Ensembl
chr8:26226404..26227142hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38739
hg19739
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277564
Samples
Known GenesPPP2R2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564640
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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