A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3828n54



Internal ID22771723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85821003..85871268hg38UCSC Ensembl
chr14:86287347..86337612hg19UCSC Ensembl
chr14:85357100..85407365hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3850266
hg1950266
hg1850266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565442, nsv565443
Samples1798860114_A, 1780862401_A, 1780862379_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3828n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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