A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544024



Internal ID21868379
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 StatusS
Merged Variantsnsv6073052
Supporting Variants
Samples
Known GenesPLCXD3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544024
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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