A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527934



Internal ID22397320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17925745..17945766hg38UCSC Ensembl
chr9:17925743..17945764hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3820022
hg1920022
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14345455, nssv14345457, nssv14345459, nssv14345460, nssv14345456, nssv14345458, nssv14345454
SamplesHG00512, NA19238, HG00731, HG00732, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527934
Frequency
Sample Size9
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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