A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673890



Internal ID9939995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:81225417..81227080hg38UCSC Ensembl
Outerchr14:81225380..81227130hg38UCSC Ensembl
Innerchr14:81691761..81693424hg19UCSC Ensembl
Outerchr14:81691724..81693474hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg381751
hg191751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5827119
SamplesNA18959
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673890
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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