A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938643



Internal ID22714026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:24021585..26049511hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382027927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv902n209
Supporting Variantsnssv17382292
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938643
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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