A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589506



Internal ID21538069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68244251..68247989hg38UCSC Ensembl
chr15:68536589..68540327hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383739
hg193739
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096196
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589506
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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