A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762224



Internal ID20538084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15615464..15615464hg38UCSC Ensembl
chr4:15617087..15617087hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285831
Samples
Known GenesFBXL5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762224
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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