A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5999243



Internal ID21908586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1485758..1485847hg38UCSC Ensembl
chr5:1485873..1485962hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544207
Samples
Known GenesLPCAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5999243
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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