A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566050



Internal ID20939121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:120047501..120047979hg38UCSC Ensembl
chr8:121059740..121060218hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277117
Samples
Known GenesDEPTOR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566050
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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