A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671269



Internal ID9937374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103956119..103961010hg38UCSC Ensembl
chr10:105715877..105720768hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg384892
hg194892
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5930066, essv5635477, essv5551805, essv5567896
SamplesNA19058, HG01389, NA18999, NA19723
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671269
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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