A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3589n71



Internal ID6321209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1207238..1586274hg19UCSC Ensembl
chr19:1158238..1537274hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv910482, nsv910447, nsv910481
SamplesIS32841, IS33601, MS13770
Known GenesADAMTSL5, APC2, ATP5D, C19orf23, C19orf24, C19orf25, C19orf26, CIRBP, DAZAP1, EFNA2, GAMT, MBD3, MEX3D, MIDN, MUM1, NDUFS7, PCSK4, PLK5, REEP6, RPS15, STK11
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv3589n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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