A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674453



Internal ID9940558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11006337..11009117hg38UCSC Ensembl
Outerchr11:11006300..11009167hg38UCSC Ensembl
Innerchr11:11027884..11030664hg19UCSC Ensembl
Outerchr11:11027847..11030714hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg382868
hg192868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5826848
SamplesNA18552
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674453
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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