A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14360471



Internal ID22143576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65364542..65371877hg38UCSC Ensembl
chr11:65132013..65139348hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg387336
hg197336
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3230165
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14360471
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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