A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510191



Internal ID20883508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66991214..66993533hg38UCSC Ensembl
chr16:67025117..67027436hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg382320
hg192320
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194343
Samples
Known GenesCES4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510191
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