A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201789



Internal ID22351041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78055219..78055279hg38UCSC Ensembl
chr11:77766265..77766325hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14372736
SamplesNA19240
Known GenesNDUFC2-KCTD14, RNU6-83P
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201789
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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