A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6359n71



Internal ID6323979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149489110..149513626hg19UCSC Ensembl
chr5:149469303..149493819hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv883025, nsv883026
SamplesMS17208, IS38403
Known GenesCSF1R, PDGFRB
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv6359n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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