A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552809



Internal ID20925936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:243608766..243609593hg38UCSC Ensembl
chr1:243772068..243772895hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38828
hg19828
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250190
Samples
Known GenesAKT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552809
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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