A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588866



Internal ID20961937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69159287..69159658hg38UCSC Ensembl
chr16:69193190..69193561hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244312
Samples
Known GenesCIRH1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588866
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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