A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5744776



Internal ID9525993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25484846..25489783hg38UCSC Ensembl
chr14:25954052..25958989hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg384938
hg194938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672057
Supporting Variants
SamplesNA19055
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5744776
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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