A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527270



Internal ID22396657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92974565..92974727hg38UCSC Ensembl
chr11:92707731..92707893hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14359400, nssv14359399
SamplesHG00513, HG00514
Known GenesMTNR1B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527270
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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