A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2727n223



Internal ID22805695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21478301..21600400hg38UCSC Ensembl
chr16:21489622..21611721hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38122100
hg19122100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6509590, nsv6511878, nsv6501992, nsv6499184, nsv6507443
Samples
Known GenesLOC100271836, METTL9, SLC7A5P2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2727n223
Frequency
Sample Size19652
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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