A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753820



Internal ID20529680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:48112917..48112917hg38UCSC Ensembl
chr14:48582120..48582120hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294369
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753820
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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