A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1221n71



Internal ID6318841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71927468..71960554hg19UCSC Ensembl
chr11:71605116..71638202hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv897908, nsv897909
SamplesSP54956, SP54988
Known GenesFOLR2, INPPL1, PHOX2A
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv1221n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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