A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3227216



Internal ID22369779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100343067..100343815hg38UCSC Ensembl
chr10:102102824..102103572hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38749
hg19749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352939
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3227216
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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