A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3230165



Internal ID22371778
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1423n152
Supporting Variantsnssv14360472, nssv14360471
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3230165
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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