A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645674



Internal ID21593979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71235429..71235429hg38UCSC Ensembl
chr14:71702146..71702146hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17088858
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645674
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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