A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv800n223



Internal ID22803768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69471033..69478254hg38UCSC Ensembl
chr10:71230789..71238010hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg387222
hg197222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6439961, nsv6454108
Samples
Known GenesTSPAN15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv800n223
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