A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602150



Internal ID21550805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52290064..52290394hg38UCSC Ensembl
chr14:52756782..52757112hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17093643
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602150
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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