A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584164



Internal ID21532700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133757569..133757645hg38UCSC Ensembl
chr8:134769812..134769888hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153218
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584164
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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