A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586966



Internal ID21535524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99128277..99128396hg38UCSC Ensembl
chr14:99594614..99594733hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091193
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586966
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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