A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5621414



Internal ID8598817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14804467..14812142hg38UCSC Ensembl
chr19:14915279..14922954hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg387676
hg197676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663270
Supporting Variants
SamplesNA19311
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5621414
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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