A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510187



Internal ID20883504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:17021501..17038800hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3817300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2363n223
Supporting Variantsnssv18190926
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510187
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