A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766731



Internal ID20542591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46466336..46466336hg38UCSC Ensembl
chr10:47083114..47083114hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295866
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766731
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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