A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579406



Internal ID20952477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50131026..50131553hg38UCSC Ensembl
chr16:50164937..50165464hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240686
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579406
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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