A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584499



Internal ID21533040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45523568..45523722hg38UCSC Ensembl
chr1:45989240..45989394hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065844
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584499
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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