A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6332n71



Internal ID6323952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:131996669..132008016hg19UCSC Ensembl
chr5:132024568..132035915hg18UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv882907, nsv882908, nsv882906, nsv882909
SamplesSP54650, SP54381, SP54614, SP52025
Known GenesIL13
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv6332n71
Frequency
Sample Size6533
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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