A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566388



Internal ID20939459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165044534..165045281hg38UCSC Ensembl
chr4:165965686..165966433hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38748
hg19748
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264920
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566388
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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