A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354299



Internal ID21011852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46023258..46027282hg38UCSC Ensembl
chr2:46250397..46254421hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg384025
hg194025
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089362
Samples
Known GenesPRKCE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354299
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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