A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081459



Internal ID21476362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24209057..24209057hg38UCSC Ensembl
chr14:24678263..24678263hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663677
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081459
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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