A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14348375



Internal ID22136936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110612026..110612026hg38UCSC Ensembl
chr9:113374306..113374306hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3565657
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14348375
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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