A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449826



Internal ID21107379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22312201..22359700hg38UCSC Ensembl
chr10:22601130..22648629hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3847500
hg1947500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv649n223
Supporting Variantsnssv18183584
Samples
Known GenesBMI1, COMMD3, COMMD3-BMI1, SPAG6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449826
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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