A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528952



Internal ID22398345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33848549..33851320hg38UCSC Ensembl
chr11:33870095..33872866hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382772
hg192772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357628, nssv14357629
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528952
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer