A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263611



Internal ID20472829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36764028..36764028hg38UCSC Ensembl
chr14:37233233..37233233hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4768113
Supporting Variants
Samples
Known GenesSLC25A21
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263611
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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