A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006213



Internal ID21915556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123012401..123015652hg38UCSC Ensembl
chr10:124771917..124775168hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg383252
hg193252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587844
Samples
Known GenesACADSB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006213
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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