A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368842



Internal ID21026395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134517811..134640184hg38UCSC Ensembl
chr3:134236653..134359026hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38122374
hg19122374
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209583
Samples
Known GenesCEP63, KY
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368842
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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