A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415779



Internal ID21073332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:15460408..15476454hg38UCSC Ensembl
chr8:15317917..15333963hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3816047
hg1916047
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222212
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415779
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