A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500635



Internal ID20873863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3639831..3644181hg38UCSC Ensembl
chr16:3689832..3694182hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg384351
hg194351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029413
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500635
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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