A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156309



Internal ID22084785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9268546..9286961hg38UCSC Ensembl
Outerchr5:9264570..9291176hg38UCSC Ensembl
Innerchr5:9268658..9287073hg19UCSC Ensembl
Outerchr5:9264682..9291288hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3826607
hg1926607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4020628
Samples
Known GenesSEMA5A
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156309
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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