A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5588709



Internal ID21537272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105739765..105739852hg38UCSC Ensembl
chr14:106206102..106206189hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090418
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5588709
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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