A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763399



Internal ID20539259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114083938..114083938hg38UCSC Ensembl
chr10:115843697..115843697hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg381896
hg191896
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280734
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763399
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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