A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663899



Internal ID21612204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71855894..71855894hg38UCSC Ensembl
chr14:72322611..72322611hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081427
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663899
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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