A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14346796



Internal ID22222649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66337937..66338003hg38UCSC Ensembl
chr9:42183748..42183802hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3867
hg1955
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3213724
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14346796
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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