A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675728



Internal ID9941833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68452138..68453498hg38UCSC Ensembl
chr10:70211895..70213255hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381361
hg191361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5582793
SamplesHG00260
Known GenesDNA2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675728
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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