A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6302314



Internal ID8930790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:102878570..102882598hg38UCSC Ensembl
Outerchr11:102878413..102882751hg38UCSC Ensembl
Innerchr11:102749300..102753328hg19UCSC Ensembl
Outerchr11:102749143..102753481hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg384339
hg194339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666963
Supporting Variants
SamplesHG00442
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6302314
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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