A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17587844



Internal ID21779887
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 StatusS
Merged Variantsnsv6006213
Supporting Variants
Samples
Known GenesACADSB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17587844
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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