A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568972



Internal ID20942043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119887476..119889699hg38UCSC Ensembl
chr8:120899716..120901939hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg382224
hg192224
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277097
Samples
Known GenesDEPTOR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568972
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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