A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678815



Internal ID9944920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21852313..21902833hg38UCSC Ensembl
chr14:22320490..22371013hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3850521
hg1950524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv384e199
Supporting Variantsessv6338027, essv6579384, essv5872537
SamplesNA19057, NA20537, NA18987
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678815
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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