A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751555



Internal ID20527415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:12654733..12654733hg38UCSC Ensembl
chr3:12696232..12696232hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg382642
hg192642
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287137
Samples
Known GenesRAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751555
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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