A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv621n223



Internal ID22803589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16451621..16478379hg38UCSC Ensembl
chr10:16493620..16520378hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3826759
hg1926759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6446133, nsv6446978
Samples
Known GenesPTER
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv621n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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