A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3426n54



Internal ID20136850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113048260..113159539hg38UCSC Ensembl
chr13:113702574..113813853hg19UCSC Ensembl
chr13:112750575..112861854hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38111280
hg19111280
hg18111280
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv563265, nsv563264
Samples
Known GenesF10, F7, MCF2L, PROZ
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3426n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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