A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222718



Internal ID22366703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20009984..20010119hg38UCSC Ensembl
chr11:20031530..20031665hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14356110
SamplesNA19240
Known GenesNAV2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222718
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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