A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898111



Internal ID22673222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:12816288..12818818hg38UCSC Ensembl
chr4:12817912..12820442hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg382531
hg192531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426269
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898111
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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