A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655161



Internal ID21603466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104653260..104653260hg38UCSC Ensembl
chr14:105119597..105119597hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090039
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655161
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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