A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589259



Internal ID20962330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75724212..76087815hg38UCSC Ensembl
chr16:75758110..76121713hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38363604
hg19363604
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240093
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589259
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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