A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1619n152



Internal ID22817322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126473080..126473131hg38UCSC Ensembl
chr11:126342975..126343026hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3202544, nsv3200576
SamplesNA19240, HG00733, HG00514
Known GenesKIRREL3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv1619n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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