A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760347



Internal ID20536207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:115698000..115698000hg38UCSC Ensembl
chr3:115416847..115416847hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279378
Samples
Known GenesGAP43
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760347
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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