A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899268



Internal ID22674396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1485724..1485815hg38UCSC Ensembl
chr5:1485839..1485930hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425176
Samples
Known GenesLPCAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899268
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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