A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335423



Internal ID20868615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:233120616..233134947hg38UCSC Ensembl
chr1:233256362..233270693hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3814332
hg1914332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058783
Samples
Known GenesPCNXL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335423
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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