A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761294



Internal ID20537154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71296928..71296928hg38UCSC Ensembl
chr10:73056685..73056685hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282065
Samples
Known GenesUNC5B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761294
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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