A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv190n67



Internal ID6316458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3838740..3839759hg19UCSC Ensembl
chr11:3795316..3796335hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv825719, nsv825718
SamplesNA18972, AK4
Known GenesPGAP2
Method
Analysis
Platform
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)dgv190n67
Frequency
Sample Size31
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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