A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671420



Internal ID9937525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:113447758..113457057hg38UCSC Ensembl
Outerchr10:113447601..113457210hg38UCSC Ensembl
Innerchr10:115207517..115216816hg19UCSC Ensembl
Outerchr10:115207360..115216969hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg389610
hg199610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv170e199
Supporting Variantsessv6508214, essv6327665
SamplesNA12045, HG00136
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671420
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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