A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588033



Internal ID20961104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69122828..69123321hg38UCSC Ensembl
chr16:69156731..69157224hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38494
hg19494
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244309
Samples
Known GenesCHTF8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588033
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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