A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566069



Internal ID21514389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:135948598..135948793hg38UCSC Ensembl
chr8:136960841..136961036hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150341
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566069
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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