A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211401



Internal ID22358973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127016789..127017104hg38UCSC Ensembl
chr10:128815053..128815368hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14355972
SamplesHG00513
Known GenesDOCK1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211401
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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