A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000116



Internal ID21909459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:41411875..41411961hg38UCSC Ensembl
chr5:41411977..41412063hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552982
Samples
Known GenesPLCXD3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000116
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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