A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3194859



Internal ID22345121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118875593..118875675hg38UCSC Ensembl
chr11:118746302..118746384hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14446498, nssv14379171
SamplesNA19240, HG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3194859
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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