A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998348



Internal ID21907691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:789914..790069hg38UCSC Ensembl
chr4:783702..783857hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555409
Samples
Known GenesCPLX1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998348
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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