A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589402



Internal ID20962473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102725666..102726219hg38UCSC Ensembl
chr10:104485423..104485976hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220815
Samples
Known GenesSFXN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589402
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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