A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569086



Internal ID21517439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42520414..42522788hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141962
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569086
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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