A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363089



Internal ID21020642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138534946..138535639hg38UCSC Ensembl
chr3:138253788..138254481hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093891
Samples
Known GenesCEP70
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363089
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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