A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558041



Internal ID20931112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:130022268..130022836hg38UCSC Ensembl
chr8:131034514..131035082hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276259
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558041
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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