A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666099



Internal ID9585518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48368190..48372669hg38UCSC Ensembl
Outerchr10:48368153..48372719hg38UCSC Ensembl
Innerchr10:49576233..49580712hg19UCSC Ensembl
Outerchr10:49576196..49580762hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg384567
hg194567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6142858
SamplesNA18633
Known GenesMAPK8
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666099
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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