A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675699



Internal ID9941804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106113331..106717641hg38UCSC Ensembl
Outerchr14:106113331..106717676hg38UCSC Ensembl
Innerchr14:106541845..107172888hg19UCSC Ensembl
Outerchr14:106541811..107172923hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38604346
hg19631113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv429e199
Supporting Variantsessv5603932
SamplesHG00155
Known GenesLINC00221, LINC00226
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675699
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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