A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3284463



Internal ID22382827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63319327..63319381hg38UCSC Ensembl
chr11:63086799..63086853hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1417n152
Supporting Variantsnssv14445432
SamplesHG00733
Known GenesMIR3680-1, MIR3680-2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3284463
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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