A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584903



Internal ID21533447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25206855..25207163hg38UCSC Ensembl
chr14:25676061..25676369hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17083079
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584903
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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