A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083558



Internal ID21464989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97235750..97235750hg38UCSC Ensembl
chr14:97702087..97702087hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661959
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083558
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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