A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567129



Internal ID20940200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54008173..54008853hg38UCSC Ensembl
chr8:54920733..54921413hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38681
hg19681
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278231
Samples
Known GenesTCEA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567129
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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