A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922386



Internal ID22697611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15157390..15159633hg38UCSC Ensembl
chr9:15157388..15159631hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg382244
hg192244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2078n209
Supporting Variantsnssv17448515
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922386
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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