A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213192



Internal ID22360212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111979174..111979534hg38UCSC Ensembl
chr9:114741454..114741814hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14349044
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213192
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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