A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154457



Internal ID22084962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21700796..21727209hg38UCSC Ensembl
Outerchr9:21696289..21730411hg38UCSC Ensembl
Innerchr9:21700795..21727208hg19UCSC Ensembl
Outerchr9:21696288..21730410hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3834123
hg1934123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4006297
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154457
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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