A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7865773



Internal ID13318061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86660941..86660953hg38UCSC Ensembl
Innerchr14:86660918..86660976hg38UCSC Ensembl
Outerchr14:86660906..86660988hg38UCSC Ensembl
chr14:87127285..87127297hg19UCSC Ensembl
Innerchr14:87127262..87127320hg19UCSC Ensembl
Outerchr14:87127250..87127332hg19UCSC Ensembl
chr14:86197038..86197050hg18UCSC Ensembl
Innerchr14:86197073..86197015hg18UCSC Ensembl
Outerchr14:86197003..86197085hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3417405
Supporting Variants
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7865773
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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