A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640328



Internal ID21588633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81350710..81350710hg38UCSC Ensembl
chr8:82262945..82262945hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148021
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640328
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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