A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580774



Internal ID21529268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59537377..59542113hg38UCSC Ensembl
chr8:60449936..60454672hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg384737
hg194737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17156536
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580774
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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