A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14358754



Internal ID22271766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:84191990..84191990hg38UCSC Ensembl
chr11:83903033..83903033hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3559710
Supporting Variants
SamplesNA19239
Known GenesDLG2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14358754
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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