A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14357015



Internal ID22268429
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528954
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14357015
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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