A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591558



Internal ID21540134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85734693..85738551hg38UCSC Ensembl
chr14:86201037..86204895hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg383859
hg193859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092275
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591558
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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