A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638297



Internal ID21586602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124309834..124309834hg38UCSC Ensembl
chr8:125322075..125322075hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17146848
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638297
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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