A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2191n54



Internal ID20135615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125205679..125223954hg38UCSC Ensembl
chr11:125075575..125093850hg19UCSC Ensembl
chr11:124580785..124599060hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3818276
hg1918276
hg1818276
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556516, nsv556497
Samples
Known GenesPKNOX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2191n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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