A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594101



Internal ID20967172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21484749..21485749hg38UCSC Ensembl
chr14:21952908..21953908hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2056n223
Supporting Variantsnssv18235254
Samples
Known GenesTOX4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594101
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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