A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3033n71



Internal ID6320653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1612199..1683012hg19UCSC Ensembl
chr17:1558949..1629762hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv907519, nsv907520
SamplesMS10311, MS17208
Known GenesMIR22, MIR22HG, SERPINF1, SERPINF2, SMYD4, TLCD2, WDR81
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv3033n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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