A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678695



Internal ID9598114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8936537..8943612hg38UCSC Ensembl
Outerchr11:8936500..8943662hg38UCSC Ensembl
Innerchr11:8958084..8965159hg19UCSC Ensembl
Outerchr11:8958047..8965209hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg387163
hg197163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv191e199
Supporting Variantsessv6090816
SamplesNA18622
Known GenesASCL3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678695
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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