A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv394n71



Internal ID6318014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158625789..158712510hg19UCSC Ensembl
chr1:156892413..156979134hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv872483, nsv872481, nsv872482
SamplesIS34805, IS36640, IS30141, MS22898
Known GenesOR6K2, OR6K3, SPTA1
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv394n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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