A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv902n209



Internal ID22826977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:23734358..26177784hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382443427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5945372, nsv5928454, nsv5930642, nsv5938643
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv902n209
Frequency
Sample Size914
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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