A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2009n71



Internal ID6319629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105086475..105311249hg19UCSC Ensembl
chr14:104157520..104382294hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv902388, nsv902396, nsv902392, nsv902394, nsv902379, nsv902387
SamplesMS12262, MS11579, IS35726, IS33162, IS33504, MS13727, IS33665
Known GenesADSSL1, AKT1, INF2, MGC23270, MIR4710, SIVA1, ZBTB42
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv2009n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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