A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14359799



Internal ID22284634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63319312..63319366hg38UCSC Ensembl
chr11:63086784..63086838hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3229391
Supporting Variants
SamplesNA19239
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14359799
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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