A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3658n54



Internal ID22771553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:40441476..40461883hg38UCSC Ensembl
chr14:40910680..40931087hg19UCSC Ensembl
chr14:39980430..40000837hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3820408
hg1920408
hg1820408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564461, nsv564460, nsv564459
SamplesHGDP00828, NINDS_97
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3658n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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