A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559628



Internal ID20932699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:120770803..120772254hg38UCSC Ensembl
chr8:121783043..121784494hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg381452
hg191452
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276058
Samples
Known GenesSNTB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559628
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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