A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528954



Internal ID22398347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:26300925..26301168hg38UCSC Ensembl
chr11:26322472..26322715hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357016, nssv14357015
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528954
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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