A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573603



Internal ID20946674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30170041..30170906hg38UCSC Ensembl
chr8:30027557..30028422hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38866
hg19866
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277673
Samples
Known GenesDCTN6, MIR548O2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573603
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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