A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv429e199



Internal ID22758202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:106113331..106773460hg38UCSC Ensembl
chr14:106541811..107181699hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38660130
hg19639889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2677059, esv2671687, esv2675699
SamplesNA20507, NA18916, NA20540, NA20539, NA18638, HG00701, HG00246, HG00155, NA19147, NA19473, HG01551, HG00607, HG00418, HG00339
Known GenesLINC00221, LINC00226
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv429e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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