A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426686



Internal ID21084239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140597101..140600900hg38UCSC Ensembl
chr8:141607200..141610999hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217287
Samples
Known GenesAGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426686
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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