A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073052



Internal ID21982285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:41373046..41373046hg38UCSC Ensembl
chr5:41373148..41373148hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544024
Samples
Known GenesPLCXD3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073052
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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