A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833055



Internal ID6158779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:74988344..75166288hg19UCSC Ensembl
Outerchr15:72775397..72953341hg18UCSC Ensembl
Outerchr15:72775397..72953341hg17UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1452022
Samples
Known GenesCPLX3, CSK, CYP1A1, CYP1A2, EDC3, LMAN1L, MIR4513, SCAMP2, ULK3
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833055
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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