A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080933



Internal ID21490236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24406201..24406201hg38UCSC Ensembl
chr14:24875407..24875407hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661044
Supporting Variants
SamplesNA19238
Known GenesNYNRIN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080933
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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