A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544127



Internal ID20917366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25767892..25768848hg38UCSC Ensembl
chr3:25809383..25810339hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38957
hg19957
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262620
Samples
Known GenesNGLY1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544127
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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