A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277630



Internal ID20844670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28939024..28939792hg38UCSC Ensembl
chr8:28796541..28797309hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38769
hg19769
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573593
Supporting Variants
Samples
Known GenesHMBOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277630
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00055


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