A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578770



Internal ID20951841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66734915..66735122hg38UCSC Ensembl
chr16:66768818..66769025hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243582
Samples
Known GenesDYNC1LI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578770
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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