A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885363



Internal ID22660347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:13818951..13819334hg38UCSC Ensembl
chr2:13959076..13959459hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397163
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885363
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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