A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3712n54



Internal ID22771607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:48316156..48451683hg38UCSC Ensembl
chr14:48785359..48920886hg19UCSC Ensembl
chr14:47855109..47990636hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38135528
hg19135528
hg18135528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564820, nsv564819, nsv564815, nsv564821, nsv564816, nsv564817
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3712n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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