A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098911



Internal ID21460919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:46591425..46591425hg38UCSC Ensembl
chr14:47060628..47060628hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655986
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098911
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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