A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3739n71



Internal ID6321359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13975377..14298442hg19UCSC Ensembl
chr19:13836377..14159442hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv911107, nsv911103
SamplesMS10311, IS39233
Known GenesASF1B, C19orf57, CC2D1A, DCAF15, IL27RA, LOC113230, LPHN1, MIR181C, MIR181D, NANOS3, PALM3, PODNL1, PRKACA, RFX1, RLN3, SAMD1
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv3739n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer