A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503845



Internal ID20877102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69129560..69151125hg38UCSC Ensembl
chr16:69163463..69185028hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3821566
hg1921566
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177587
Samples
Known GenesCHTF8, CIRH1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503845
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