A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659492



Internal ID9925597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:98568335..98590951hg38UCSC Ensembl
Outerchr14:98568298..98591001hg38UCSC Ensembl
Innerchr14:99034672..99057288hg19UCSC Ensembl
Outerchr14:99034635..99057338hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3822704
hg1922704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5510000, essv6368545
SamplesNA19332, NA19108
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659492
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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