A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv37n68



Internal ID6317562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88833868..89011311hg19UCSC Ensembl
chr16:87361369..87538812hg18UCSC Ensembl
chr16:87361369..87538812hg17UCSC Ensembl
Cytoband16q24.3
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 Variantsnsv833329, nsv833328
Samples
Known GenesAPRT, CBFA2T3, CDT1, GALNS, PABPN1L, PIEZO1, TRAPPC2L
Method
Analysis
Platform
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)dgv37n68
Frequency
Sample Size95
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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