A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14360972



Internal ID22253065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134259357..134259469hg38UCSC Ensembl
chr11:134129251..134129363hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3211515
Supporting Variants
SamplesNA19238
Known GenesACAD8
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14360972
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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