A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223039



Internal ID22366926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36055104..36055236hg38UCSC Ensembl
chr11:36076654..36076786hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357679, nssv14357680
SamplesHG00731, HG00732
Known GenesLDLRAD3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223039
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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