A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652563



Internal ID21600868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51751339..51751339hg38UCSC Ensembl
chr14:52218057..52218057hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082482
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652563
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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