A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3951n71



Internal ID6321571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45816547..45827194hg19UCSC Ensembl
chr19:50508387..50519034hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv912149, nsv912148
SamplesSP54726, SP80957
Known GenesCKM
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv3951n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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