A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220536



Internal ID22365202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35222309..35237978hg38UCSC Ensembl
chr11:35243856..35259525hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3815670
hg1915670
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357674, nssv14357675
SamplesHG00512, HG00514
Known GenesCD44
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220536
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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