A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3227981



Internal ID22370305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120516931..120517656hg38UCSC Ensembl
chr11:120387640..120388365hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38726
hg19726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14361372, nssv14361373
SamplesNA19239, NA19240
Known GenesGRIK4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3227981
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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