A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3412182



Internal ID15259141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58105691..58105704hg38UCSC Ensembl
Innerchr14:58105693..58105702hg38UCSC Ensembl
Outerchr14:58105689..58105706hg38UCSC Ensembl
chr14:58572409..58572422hg19UCSC Ensembl
Innerchr14:58572411..58572420hg19UCSC Ensembl
Outerchr14:58572407..58572424hg19UCSC Ensembl
chr14:57642162..57642175hg18UCSC Ensembl
Innerchr14:57642164..57642173hg18UCSC Ensembl
Outerchr14:57642160..57642177hg18UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7865737
SamplesNA12005
Known GenesC14orf37
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3412182
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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