A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5610574



Internal ID9625176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107367690..107374496hg38UCSC Ensembl
Outerchr11:107367319..107374866hg38UCSC Ensembl
Innerchr11:107238416..107245222hg19UCSC Ensembl
Outerchr11:107238045..107245592hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg387548
hg197548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665722
Supporting Variants
SamplesNA19338
Known GenesCWF19L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5610574
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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