A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652088



Internal ID21600393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65385997..65385997hg38UCSC Ensembl
chr14:65852715..65852715hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080770
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652088
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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