A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3746n54



Internal ID22771641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70220199..70222673hg38UCSC Ensembl
chr14:70686916..70689390hg19UCSC Ensembl
chr14:69756669..69759143hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg382475
hg192475
hg182475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565012, nsv565010, nsv565013, nsv565011
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3746n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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