A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760118



Internal ID20535978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64843586..64843586hg38UCSC Ensembl
chr15:65135785..65135785hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269075
Samples
Known GenesPLEKHO2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760118
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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