A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221768



Internal ID22366040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18528045..18528376hg38UCSC Ensembl
chr11:18549592..18549923hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14355471, nssv14355469, nssv14355470
SamplesHG00512, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221768
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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