A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568954



Internal ID20942025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138157386..138843464hg38UCSC Ensembl
chr3:137876228..138562306hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38686079
hg19686079
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259707
Samples
Known GenesARMC8, CEP70, DBR1, ESYT3, FAIM, MRAS, NME9, PIK3CB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568954
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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