A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833777



Internal ID6159501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:18875936..19031076hg19UCSC Ensembl
Outerchr19:18736936..18892076hg18UCSC Ensembl
Outerchr19:18736936..18892076hg17UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1454611, nssv1454612
Samples
Known GenesCERS1, COMP, COPE, CRTC1, DDX49, GDF1, UPF1
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833777
Frequency
Sample Size95
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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