A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277672



Internal ID20844712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30163330..30163449hg38UCSC Ensembl
chr8:30020846..30020965hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560645
Supporting Variants
Samples
Known GenesDCTN6, MIR548O2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277672
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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