A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229139



Internal ID22371078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68372261..68372391hg38UCSC Ensembl
chr11:68139729..68139859hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1434n152
Supporting Variantsnssv14360597
SamplesHG00733
Known GenesLRP5
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229139
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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