A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14348263



Internal ID22226047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107388994..107390016hg38UCSC Ensembl
chr9:110151275..110152297hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381023
hg191023
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3214419
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14348263
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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