A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154518



Internal ID22085023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:86207833..86227936hg38UCSC Ensembl
Outerchr9:86203367..86231000hg38UCSC Ensembl
Innerchr9:88822748..88842851hg19UCSC Ensembl
Outerchr9:88818282..88845915hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3827634
hg1927634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4006670, nssv4006669
Samples
Known GenesC9orf153
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154518
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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