A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14390911



Internal ID22129116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60815916..60815916hg38UCSC Ensembl
chr15:61108115..61108115hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3561041
Supporting Variants
SamplesHG00512
Known GenesRORA
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14390911
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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