A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3867n54



Internal ID20137291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96623270..96671344hg38UCSC Ensembl
chr14:97089607..97137681hg19UCSC Ensembl
chr14:96159360..96207434hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3848075
hg1948075
hg1848075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565651, nsv565650
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3867n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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