A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417552



Internal ID21075105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53290190..53316064hg38UCSC Ensembl
chr8:54202750..54228624hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3825875
hg1925875
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236454
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417552
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer