A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14360637



Internal ID22301214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116119737..116119737hg38UCSC Ensembl
chr11:115990454..115990454hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3559211
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14360637
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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