A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2977n71



Internal ID6320597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88688435..88807205hg19UCSC Ensembl
chr16:87215936..87334706hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv907274, nsv907269, nsv907279, nsv907284
SamplesIS39258, MS10123, IS39417, MS10386
Known GenesCTU2, CYBA, IL17C, MGC23284, MIR4722, MVD, PIEZO1, RNF166, SNAI3, ZC3H18
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv2977n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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