A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568514



Internal ID21516863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26239551..26239613hg38UCSC Ensembl
chr1:26566042..26566104hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17064302
SamplesNA19238
Known GenesCEP85
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568514
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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