A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222128



Internal ID22366303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57717015..57717131hg38UCSC Ensembl
chr11:57484487..57484603hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14358888
SamplesNA19239
Known GenesTMX2, TMX2-CTNND1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222128
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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