A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276988



Internal ID20844028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11431141..11714759hg38UCSC Ensembl
chr8:11288650..11572268hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38283619
hg19283619
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562393
Supporting Variants
Samples
Known GenesBLK, C8orf12, FAM167A, GATA4, LINC00208
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276988
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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