A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596038



Internal ID21544645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47133509..47133635hg38UCSC Ensembl
chr15:47425707..47425833hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085018
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596038
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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