A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4005295



Internal ID22066926
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154482
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4005295
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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