A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226460



Internal ID22369253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15594012..15598679hg38UCSC Ensembl
chr11:15615558..15620225hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg384668
hg194668
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14355362, nssv14355363, nssv14355361
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226460
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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