A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567814



Internal ID20940885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:133963406..133964071hg38UCSC Ensembl
chr6:134284544..134285209hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38666
hg19666
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271912
Samples
Known GenesTBPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567814
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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