A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562393



Internal ID20935464
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 StatusM
Merged Variants
Supporting Variantsnssv18276988
Samples
Known GenesBLK, C8orf12, FAM167A, GATA4, LINC00208
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562393
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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