A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv412n71



Internal ID6318032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:186640853..186643541hg19UCSC Ensembl
chr1:184907476..184910164hg18UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv872591, nsv872594
SamplesSP50120, SP50144
Known GenesPTGS2
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv412n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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