A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv185n71



Internal ID6317805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17267496..17344279hg19UCSC Ensembl
chr1:17140083..17216866hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv870569, nsv870461, nsv871088
SamplesSP54956, IS39417, MS10311, IS39233, MS10698, MS10769
Known GenesATP13A2, CROCC, MFAP2
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv185n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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