A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154470



Internal ID22084975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:27426465..27433425hg38UCSC Ensembl
Outerchr9:27423977..27435276hg38UCSC Ensembl
Innerchr9:27426463..27433423hg19UCSC Ensembl
Outerchr9:27423975..27435274hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3811300
hg1911300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007024
Samples
Known GenesMOB3B
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154470
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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