A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154482



Internal ID22084987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38486214..38498484hg38UCSC Ensembl
Outerchr9:38485986..38500229hg38UCSC Ensembl
Innerchr9:38486211..38498481hg19UCSC Ensembl
Outerchr9:38485983..38500226hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3814244
hg1914244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005295
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154482
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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