A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5592343



Internal ID21540924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24391770..24392075hg38UCSC Ensembl
chr14:24860976..24861281hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092597
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5592343
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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