A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11526n54



Internal ID22779421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99863860..99865757hg38UCSC Ensembl
chr7:99461483..99463380hg19UCSC Ensembl
chr7:99299419..99301316hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381898
hg191898
hg181898
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607927, nsv607926
Samples
Known GenesCYP3A43
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11526n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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