A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568434



Internal ID21516782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131363266..131363336hg38UCSC Ensembl
chr6:131684406..131684476hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158421
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568434
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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