A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900731



Internal ID22675876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24809806..24810262hg38UCSC Ensembl
chr6:24810034..24810490hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446616
Samples
Known GenesFAM65B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900731
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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