A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673556



Internal ID9939661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:26633330..26677377hg38UCSC Ensembl
chr14:27102536..27146583hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3844048
hg1944048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5550641
SamplesHG01174
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673556
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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