A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5468308



Internal ID9141436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:97315036..97324458hg38UCSC Ensembl
Outerchr3:97314987..97324508hg38UCSC Ensembl
Innerchr3:97033880..97043302hg19UCSC Ensembl
Outerchr3:97033831..97043352hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg389522
hg199522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666202
Supporting Variants
SamplesHG01188
Known GenesEPHA6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5468308
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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