A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv388e199



Internal ID22758161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32868319..32881887hg38UCSC Ensembl
chr14:33337525..33351093hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3813569
hg1913569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2657339, esv2669888
SamplesHG01365
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv388e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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