A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568439



Internal ID21516787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66618441..66624225hg38UCSC Ensembl
chr8:67530676..67536460hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg385785
hg195785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158971
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568439
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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