A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6306018



Internal ID9283421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67139916..67149786hg38UCSC Ensembl
Outerchr11:67139759..67149939hg38UCSC Ensembl
Innerchr11:66907387..66917257hg19UCSC Ensembl
Outerchr11:66907230..66917410hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3810181
hg1910181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661599
Supporting Variants
SamplesHG00367
Known GenesKDM2A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6306018
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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