A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559204



Internal ID22428008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10802029..10802029hg38UCSC Ensembl
chr11:10823576..10823576hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14354637, nssv14354642, nssv14354638, nssv14354640, nssv14354639, nssv14354636, nssv14354634, nssv14354641, nssv14354635
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesEIF4G2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559204
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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