A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213081



Internal ID22360137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1656501..1669500hg38UCSC Ensembl
chr11:1677731..1690730hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3813000
hg1913000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357174, nssv14357172, nssv14357177, nssv14357178, nssv14357180, nssv14357175, nssv14357173, nssv14357176, nssv14357179
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesFAM99A, MOB2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213081
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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