A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210054



Internal ID22358035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106390904..106391105hg38UCSC Ensembl
chr3:106109751..106109952hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14307682
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210054
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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