A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1291n100



Internal ID20152907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125199208..125213796hg38UCSC Ensembl
chr11:125069104..125083692hg19UCSC Ensembl
chr11:124574314..124588902hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3814589
hg1914589
hg1814589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1042465, nsv1036414
Samples
Known GenesPKNOX2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1291n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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