A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3197409



Internal ID22347296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35606381..35606524hg38UCSC Ensembl
chr11:35627929..35628072hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14416314
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3197409
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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