A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675397



Internal ID9941502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9801227..9802968hg38UCSC Ensembl
chr19:9911903..9913644hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381742
hg191742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5715666
SamplesHG00233
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675397
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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