A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11290n54



Internal ID20144714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40153936..40320658hg38UCSC Ensembl
chr7:40193535..40360257hg19UCSC Ensembl
chr7:40160060..40326782hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38166723
hg19166723
hg18166723
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv606710, nsv606711
Samples
Known GenesC7orf10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11290n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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