A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5594277



Internal ID21542874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88513782..88514097hg38UCSC Ensembl
chr15:89057013..89057328hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081224
SamplesHG03125
Known GenesDET1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5594277
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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