A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757449



Internal ID20533309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22674302..22674302hg38UCSC Ensembl
chr8:22531815..22531815hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757449
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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