A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591341



Internal ID21539916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64799168..64799247hg38UCSC Ensembl
chr15:65091367..65091446hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086369
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591341
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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