A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10273n54



Internal ID22778168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3143886..3146800hg38UCSC Ensembl
chr6:3144120..3147034hg19UCSC Ensembl
chr6:3089119..3092033hg18UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg382915
hg192915
hg182915
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600837, nsv600838
Samples
Known GenesBPHL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10273n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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