A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626006



Internal ID21574311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42766494..42766494hg38UCSC Ensembl
chr8:42621637..42621637hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154146
SamplesNA19238
Known GenesCHRNA6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626006
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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