A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276054



Internal ID20843094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:120578147..120579125hg38UCSC Ensembl
chr8:121590387..121591365hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38979
hg19979
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559553
Supporting Variants
Samples
Known GenesSNTB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276054
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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