A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945372



Internal ID22720848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:23855154..26177784hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382322631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv902n209
Supporting Variantsnssv17388206
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945372
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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