A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218193



Internal ID22363616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73462807..73463071hg38UCSC Ensembl
chr11:73173852..73174116hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1464n152
Supporting Variantsnssv14357861, nssv14357860
SamplesHG00512, NA19240
Known GenesFAM168A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218193
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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