A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14357649



Internal ID22259596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34093854..34093854hg38UCSC Ensembl
chr11:34115401..34115401hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3559434
Supporting Variants
SamplesNA19238
Known GenesCAPRIN1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14357649
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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