A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669552



Internal ID9935657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:26475727..26481725hg38UCSC Ensembl
Outerchr13:26475690..26481775hg38UCSC Ensembl
Innerchr13:27049864..27055862hg19UCSC Ensembl
Outerchr13:27049827..27055912hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg386086
hg196086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5619178
SamplesNA18559
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669552
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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