A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277675



Internal ID20844715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30185775..30188177hg38UCSC Ensembl
chr8:30043291..30045693hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg382403
hg192403
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557254
Supporting Variants
Samples
Known GenesMIR548O2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277675
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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