A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220286



Internal ID22365021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70173791..70174240hg38UCSC Ensembl
chr11:70019897..70020346hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357755, nssv14357756, nssv14357134
SamplesNA19238, NA19239, HG00733
Known GenesANO1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220286
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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