A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213222



Internal ID22360231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1684401..1697250hg38UCSC Ensembl
chr11:1705631..1718480hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3812850
hg1912850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1231n152
Supporting Variantsnssv14376725
SamplesNA19240
Known GenesFAM99B, KRTAP5-6, MOB2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213222
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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