A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508510



Internal ID20881812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:46944273..46945984hg38UCSC Ensembl
chr16:46978185..46979896hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg381712
hg191712
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185016
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508510
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