A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387909



Internal ID21045462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1500946..1501294hg38UCSC Ensembl
chr5:1501061..1501409hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128630
Samples
Known GenesLPCAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387909
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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