A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14358717



Internal ID22268776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82841053..82841053hg38UCSC Ensembl
chr11:82552095..82552095hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3559490
Supporting Variants
SamplesNA19238
Known GenesPRCP
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14358717
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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