A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214453



Internal ID22361109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10300467..10300881hg38UCSC Ensembl
chr11:10322014..10322428hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14358833, nssv14358832, nssv14358834, nssv14358835, nssv14358838, nssv14358836, nssv14358837
SamplesNA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214453
Frequency
Sample Size9
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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