A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228926



Internal ID22370946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121910866..121910997hg38UCSC Ensembl
chr11:121781574..121781705hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1602n152
Supporting Variantsnssv14361402, nssv14361403, nssv14361404
SamplesHG00731, HG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228926
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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