A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3314n54



Internal ID22771209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91347483..91349096hg38UCSC Ensembl
chr13:91999737..92001350hg19UCSC Ensembl
chr13:90797738..90799351hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg381614
hg191614
hg181614
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562698, nsv562699
Samples
Known GenesMIR17HG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3314n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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