A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424882



Internal ID21082435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41478312..41920906hg38UCSC Ensembl
chr8:41335831..41778424hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38442595
hg19442594
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229290
Samples
Known GenesAGPAT6, ANK1, GINS4, GOLGA7, MIR486, MIR486-2, NKX6-3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424882
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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