A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668656



Internal ID9934761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:100201868..100203252hg38UCSC Ensembl
Outerchr13:100201831..100203302hg38UCSC Ensembl
Innerchr13:100854122..100855506hg19UCSC Ensembl
Outerchr13:100854085..100855556hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg381472
hg191472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6327909
SamplesHG00534
Known GenesPCCA
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668656
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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