A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156317



Internal ID22084793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15709189..15720488hg38UCSC Ensembl
Outerchr5:15705211..15723237hg38UCSC Ensembl
Innerchr5:15709298..15720597hg19UCSC Ensembl
Outerchr5:15705320..15723346hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3818027
hg1918027
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4020716
Samples
Known GenesFBXL7
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156317
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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