A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659436



Internal ID21607741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:54203810..54203810hg38UCSC Ensembl
chr14:54670528..54670528hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082474
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659436
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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