A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766516



Internal ID20542376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25963105..25963105hg38UCSC Ensembl
chr4:25964727..25964727hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg382758
hg192758
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292053
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766516
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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