A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217041



Internal ID22362832
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 Variantsnssv14446531
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217041
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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