A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634574



Internal ID21582879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9670330..9670330hg38UCSC Ensembl
chr8:9527840..9527840hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142925
SamplesHG00513
Known GenesTNKS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634574
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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