A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3249141



Internal ID22377187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58627424..58631105hg38UCSC Ensembl
chr16:58661328..58665009hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg383682
hg193682
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14377268, nssv14390310, nssv14377086, nssv14378830
SamplesNA19238, HG00731, HG00732, HG00733
Known GenesCNOT1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3249141
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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