A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369899



Internal ID21027452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41268648..41694540hg38UCSC Ensembl
chr3:41310139..41736032hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38425893
hg19425894
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4851n223
Supporting Variantsnssv18099212
Samples
Known GenesULK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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