A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3698n54



Internal ID22771593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:46308006..46489633hg38UCSC Ensembl
chr14:46777209..46958836hg19UCSC Ensembl
chr14:45846959..46028586hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38181628
hg19181628
hg18181628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564743, nsv564742, nsv564741
Samples
Known GenesLINC00871
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3698n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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