A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563611



Internal ID20936682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:108250747..108251663hg38UCSC Ensembl
chr8:109262976..109263892hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38917
hg19917
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276400
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563611
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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