A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891558



Internal ID22666598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1471857..1471958hg38UCSC Ensembl
chr5:1471972..1472073hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413666
Samples
Known GenesLPCAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891558
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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