A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677524



Internal ID9943629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:33775895..33780297hg38UCSC Ensembl
Outerchr11:33775738..33780450hg38UCSC Ensembl
Innerchr11:33797441..33801843hg19UCSC Ensembl
Outerchr11:33797284..33801996hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg384713
hg194713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5951928
SamplesHG00657
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677524
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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