A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429391



Internal ID21086944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18664901..18672100hg38UCSC Ensembl
chr8:18522411..18529610hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231758
Samples
Known GenesPSD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429391
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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