A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191620



Internal ID22342300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56703270..56714333hg38UCSC Ensembl
chr11:56470746..56481809hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3811064
hg1911064
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1393n152
Supporting Variantsnssv14441605
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)nsv3191620
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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