A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210986



Internal ID22358695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65216657..65216724hg38UCSC Ensembl
chr11:64984128..64984195hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1422n152
Supporting Variantsnssv14385810
SamplesNA19240
Known GenesSLC22A20
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210986
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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