A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191394



Internal ID22342106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:21262871..21262961hg38UCSC Ensembl
chr11:21284417..21284507hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14415383
SamplesHG00514
Known GenesNELL1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3191394
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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