A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276167



Internal ID20843207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124894201..124895206hg38UCSC Ensembl
chr8:125906443..125907448hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg381006
hg191006
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564502
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276167
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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