A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752865



Internal ID20528725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78993248..78993248hg38UCSC Ensembl
chr15:79285590..79285590hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38559
hg19559
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266099
Samples
Known GenesRASGRF1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752865
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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