A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14349765



Internal ID22276900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101551616..101551616hg38UCSC Ensembl
chr9:104313898..104313898hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3565506
Supporting Variants
SamplesNA19239
Known GenesRNF20
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14349765
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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