A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5598866



Internal ID21547496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97221511..97221564hg38UCSC Ensembl
chr14:97687848..97687901hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17093196
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5598866
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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