A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511755



Internal ID20885085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23739833..23749353hg38UCSC Ensembl
chr16:23751154..23760674hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg389521
hg199521
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190885
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511755
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