A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5565850



Internal ID9327594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:66116676..66117107hg38UCSC Ensembl
Outerchr11:66116519..66117260hg38UCSC Ensembl
Innerchr11:65884147..65884578hg19UCSC Ensembl
Outerchr11:65883990..65884731hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661166
Supporting Variants
SamplesNA18522
Known GenesPACS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5565850
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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