A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588703



Internal ID20961774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69064464..69064632hg38UCSC Ensembl
chr16:69098367..69098535hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244307
Samples
Known GenesTANGO6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588703
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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