A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573028



Internal ID21521425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1511410..1511478hg38UCSC Ensembl
chr5:1511525..1511593hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137731
SamplesHG03486
Known GenesLPCAT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573028
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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