A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540745



Internal ID20914035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225833966..225835405hg38UCSC Ensembl
chr1:226021667..226023106hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg381440
hg191440
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249421
Samples
Known GenesEPHX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540745
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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