A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579934



Internal ID20953005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69376999..69377332hg38UCSC Ensembl
chr16:69410902..69411235hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244335
Samples
Known GenesTERF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579934
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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