A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389437



Internal ID21380572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68512340..68512661hg38UCSC Ensembl
chr10:70272097..70272418hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15704899
Samples
Known GenesSLC25A16
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389437
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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