A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527626



Internal ID22397013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130418176..130418282hg38UCSC Ensembl
chr11:130288071..130288177hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14362305, nssv14362304
SamplesNA19239, NA19240
Known GenesADAMTS8
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527626
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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