A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568853



Internal ID20941924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124571780..124572836hg38UCSC Ensembl
chr8:125584021..125585077hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg381057
hg191057
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276161
Samples
Known GenesMTSS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568853
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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