A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3425n54



Internal ID22771320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113031340..113083861hg38UCSC Ensembl
chr13:113685654..113738175hg19UCSC Ensembl
chr13:112733655..112786176hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3852522
hg1952522
hg1852522
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv563263, nsv563262
Samples
Known GenesMCF2L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3425n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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