A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885130



Internal ID22660114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16015194..16015301hg38UCSC Ensembl
chr2:16155316..16155423hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402503
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885130
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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