A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3391n54



Internal ID22771286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110189806..110199873hg38UCSC Ensembl
chr13:110842153..110852220hg19UCSC Ensembl
chr13:109640154..109650221hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3810068
hg1910068
hg1810068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv563103, nsv563102
SamplesHGDP00857, HGDP00868
Known GenesCOL4A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3391n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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