A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565762



Internal ID20938833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30178282..30178835hg38UCSC Ensembl
chr8:30035798..30036351hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277674
Samples
Known GenesDCTN6, MIR548O2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565762
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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