A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595238



Internal ID20968309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69127344..69127410hg38UCSC Ensembl
chr16:69161247..69161313hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244310
Samples
Known GenesCHTF8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595238
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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