A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759176



Internal ID20535036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187795358..187795358hg38UCSC Ensembl
chr3:187513146..187513146hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268303
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759176
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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