A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760659



Internal ID20536519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13241643..13241643hg38UCSC Ensembl
chr10:13283643..13283643hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760659
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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