A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1405n152



Internal ID22817108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60982123..60982174hg38UCSC Ensembl
chr11:60749595..60749646hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3198386, nsv3205034
SamplesNA19240, HG00733, HG00514
Known GenesCD6
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv1405n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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