A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015650



Internal ID21924993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30388398..30388638hg38UCSC Ensembl
chr8:30245914..30246154hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557849
Samples
Known GenesRBPMS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015650
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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