A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223294



Internal ID22367110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102703426..102704152hg38UCSC Ensembl
chr10:104463183..104463909hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38727
hg19727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14353620
SamplesHG00731
Known GenesARL3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223294
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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