A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666644



Internal ID9932749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4808058..4814041hg38UCSC Ensembl
Outerchr19:4808021..4814091hg38UCSC Ensembl
Innerchr19:4808070..4814053hg19UCSC Ensembl
Outerchr19:4808033..4814103hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg386071
hg196071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5636129
SamplesHG01047
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666644
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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