A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598550



Internal ID21790595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36789776..36789776hg38UCSC Ensembl
chr14:37258981..37258981hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6095431
Supporting Variants
Samples
Known GenesSLC25A21
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598550
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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