A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552569



Internal ID20925694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:53332771..53333390hg38UCSC Ensembl
chr3:53366798..53367417hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261438
Samples
Known GenesDCP1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552569
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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