A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660473



Internal ID9926578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6726651..6728140hg38UCSC Ensembl
chr19:6726662..6728151hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381490
hg191490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5429217
SamplesNA19399
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660473
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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