A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5592691



Internal ID21541274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20309952..20310027hg38UCSC Ensembl
chr14:20778111..20778186hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098702
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5592691
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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