A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666707



Internal ID9586126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6229270..6229660hg38UCSC Ensembl
Outerchr19:6229233..6229710hg38UCSC Ensembl
Innerchr19:6229281..6229671hg19UCSC Ensembl
Outerchr19:6229244..6229721hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6310241
SamplesNA19678
Known GenesMLLT1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666707
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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