A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429135



Internal ID21086688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18445562..18637334hg38UCSC Ensembl
chr8:18303072..18494844hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38191773
hg19191773
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217364
Samples
Known GenesPSD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429135
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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