A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2094n54



Internal ID20135518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92907621..93148767hg38UCSC Ensembl
chr11:92640787..92881933hg19UCSC Ensembl
chr11:92280435..92521581hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38241147
hg19241147
hg18241147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555904, nsv555903
Samples
Known GenesMTNR1B, SLC36A4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2094n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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