A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568654



Internal ID20941725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:120760230..120761617hg38UCSC Ensembl
chr8:121772470..121773857hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg381388
hg191388
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276057
Samples
Known GenesSNTB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568654
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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