A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596061



Internal ID21544668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:15284154..15284560hg38UCSC Ensembl
chr14:19129822..19130228hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38407
hg19407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130068
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596061
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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