A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767594



Internal ID20543454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36789695..36789695hg38UCSC Ensembl
chr14:37258900..37258900hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269742
Samples
Known GenesSLC25A21
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767594
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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