A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5599100



Internal ID21547733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98356257..98356333hg38UCSC Ensembl
chr14:98822594..98822670hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17097975
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5599100
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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