A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661466



Internal ID9927571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:108347598..108353388hg38UCSC Ensembl
Outerchr13:108347561..108353438hg38UCSC Ensembl
Innerchr13:108999946..109005736hg19UCSC Ensembl
Outerchr13:108999909..109005786hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg385878
hg195878
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6467749
SamplesHG00421
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661466
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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