A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568773



Internal ID20941844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140410282..140411552hg38UCSC Ensembl
chr8:141420381..141421651hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg381271
hg191271
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277258
Samples
Known GenesTRAPPC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568773
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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