A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3227372



Internal ID22369891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29644395..29644468hg38UCSC Ensembl
chr11:29665942..29666015hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14356845
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3227372
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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