A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14362957



Internal ID22328406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131295396..131295530hg38UCSC Ensembl
chr11:131165291..131165425hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3215392
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14362957
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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