A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566514



Internal ID21514841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1513648..1513701hg38UCSC Ensembl
chr5:1513763..1513816hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130295
SamplesHG03486
Known GenesLPCAT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566514
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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