A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005399



Internal ID21914742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17290545..17357076hg38UCSC Ensembl
chr6:17290776..17357307hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3866532
hg1966532
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564920
Samples
Known GenesRBM24
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005399
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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