A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217198



Internal ID22362935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74139959..74140083hg38UCSC Ensembl
chr11:73851004..73851128hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357874
SamplesNA19238
Known GenesC2CD3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217198
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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