A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674917



Internal ID9594336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132209504..132211551hg38UCSC Ensembl
Outerchr11:132209467..132211601hg38UCSC Ensembl
Innerchr11:132079398..132081445hg19UCSC Ensembl
Outerchr11:132079361..132081495hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg382135
hg192135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6142820
SamplesNA12717
Known GenesNTM
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674917
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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