A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657196



Internal ID9923301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98640764..98642609hg38UCSC Ensembl
chr13:99293018..99294863hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg381846
hg191846
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6151599
SamplesNA19379
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657196
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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