A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752083



Internal ID20527943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4149397..4149397hg38UCSC Ensembl
chr10:4191589..4191589hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283695
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752083
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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