A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3257n54



Internal ID20136681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75635643..75636856hg38UCSC Ensembl
chr13:76209779..76210992hg19UCSC Ensembl
chr13:75107780..75108993hg18UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg381214
hg191214
hg181214
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562353, nsv562351, nsv562349
Samples
Known GenesLMO7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3257n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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