A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3590n71



Internal ID6321210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1208289..1257271hg19UCSC Ensembl
chr19:1159289..1208271hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv910456, nsv910450, nsv910457, nsv910453, nsv910455
SamplesSP54935, SP55019, SP54591, SP55318, SP54967
Known GenesATP5D, C19orf26, MIDN, STK11
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv3590n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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