A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568529



Internal ID20941600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140230428..140231501hg38UCSC Ensembl
chr8:141240527..141241600hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg381074
hg191074
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277249
Samples
Known GenesTRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568529
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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