A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899009



Internal ID22674134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:91561335..93346588hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381785254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1500n209
Supporting Variantsnssv17422328
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899009
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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