A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5649733



Internal ID21598038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64907321..64907321hg38UCSC Ensembl
chr14:65374039..65374039hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17093061
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5649733
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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