A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3691n54



Internal ID22771586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:44609773..44742112hg38UCSC Ensembl
chr14:45078976..45211315hg19UCSC Ensembl
chr14:44148726..44281065hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38132340
hg19132340
hg18132340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564699, nsv564697, nsv564696, nsv564698
Samples1798860587_A, 1780862584_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3691n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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