A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3961n71



Internal ID6321581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47090085..47295652hg19UCSC Ensembl
chr19:51781925..51987492hg18UCSC 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 Variantsnsv912187, nsv912188
SamplesMS10311, MS17208, MS16153, IS39233
Known GenesCALM3, DACT3, FKRP, GNG8, LOC100506012, LOC100506068, MIR320E, PRKD2, PTGIR, SLC1A5, STRN4
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv3961n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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