A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638240



Internal ID21586545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:77805847..77805847hg38UCSC Ensembl
chr6:78515564..78515564hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg382274
hg192274
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145910
SamplesNA19239
Known GenesMEI4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638240
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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