A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360289



Internal ID21017842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132553840..132563349hg38UCSC Ensembl
chr3:132272684..132282193hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg389510
hg199510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094177
Samples
Known GenesACAD11, NPHP3-ACAD11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360289
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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