A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3648n54



Internal ID22771543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38475617..38569077hg38UCSC Ensembl
chr14:38944821..39038281hg19UCSC Ensembl
chr14:38014572..38108032hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3893461
hg1993461
hg1893461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564411, nsv564413, nsv564412, nsv564410
SamplesHGDP00810
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3648n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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