A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568432



Internal ID21516780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85179851..85180769hg38UCSC Ensembl
chr8:86092086..86093004hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38919
hg19919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141830
SamplesHG03009
Known GenesE2F5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568432
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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