A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192029



Internal ID22342665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70411210..70411260hg38UCSC Ensembl
chr11:70257316..70257366hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14387966
SamplesNA19240
Known GenesCTTN
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192029
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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