A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652811



Internal ID21601116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58753666..58753666hg38UCSC Ensembl
chr14:59220384..59220384hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg386071
hg196071
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081643
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652811
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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