A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5825330



Internal ID9422065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:625216..627822hg38UCSC Ensembl
Outerchr11:624845..628192hg38UCSC Ensembl
Innerchr11:625216..627822hg19UCSC Ensembl
Outerchr11:624845..628192hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg383348
hg193348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668299
Supporting Variants
SamplesNA18622
Known GenesCDHR5, SCT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5825330
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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