A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14357297



Internal ID22276029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3131531..3131591hg38UCSC Ensembl
chr11:3152761..3152821hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3214382
Supporting Variants
SamplesNA19239
Known GenesOSBPL5
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14357297
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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