A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5694120



Internal ID8671523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8936479..8943572hg38UCSC Ensembl
Outerchr11:8936445..8943607hg38UCSC Ensembl
Innerchr11:8958026..8965119hg19UCSC Ensembl
Outerchr11:8957992..8965154hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg387163
hg197163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665061
Supporting Variants
SamplesNA18622
Known GenesASCL3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5694120
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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