A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580435



Internal ID21528925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41442871..41442925hg38UCSC Ensembl
chr8:41300390..41300444hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142803
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580435
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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