A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591832



Internal ID21540410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82254778..82254949hg38UCSC Ensembl
chr15:82547119..82547290hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082452
SamplesHG03065
Known GenesEFTUD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591832
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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