A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093193



Internal ID21501189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36810878..36810878hg38UCSC Ensembl
chr14:37280083..37280083hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663679
Supporting Variants
SamplesNA19239
Known GenesSLC25A21
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093193
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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