A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11584n54



Internal ID20145008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114432388..114507162hg38UCSC Ensembl
chr7:114072443..114147217hg19UCSC Ensembl
chr7:113859679..113934453hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3874775
hg1974775
hg1874775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv608234, nsv608235, nsv608236
SamplesHGDP00043
Known GenesFOXP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11584n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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